Amoxicillin: Difference between revisions

Amoxicillin
	Adult Indications & Dosage
	Pediatric Indications & Dosage
	Contraindications
	Warnings & Precautions
	Adverse Reactions
	Drug Interactions
	Use in Specific Populations
	Administration & Monitoring
	Overdosage
	Pharmacology
	Clinical Studies
	How Supplied
	Images
	Patient Counseling Information
	Precautions with Alcohol
	Brand Names
	Look-Alike Names

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Revision as of 14:17, 16 December 2014

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1];

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Overview

Amoxicillin is an antibiotic that is FDA approved for the treatment of Amoxicillin is indicated in the treatment of infections due to susceptible (ONLY β-lactamase-negative) strains of the designated microorganisms in the conditions listed below:

Infections of the ear, nose, and throat - due to Streptococcus spp. (α- and β-hemolytic strains only), S. pneumoniae, Staphylococcus spp., or H. influenzae.
Infections of the genitourinary tract - due to E. coli, P. mirabilis, or E. faecalis.
Infections of the skin and skin structure - due to Streptococcus spp. (α- and β-hemolytic strains only), Staphylococcus spp., or E. coli.
Infections of the lower respiratory tract -due to Streptococcus spp. (α- and β-hemolytic strains only), S. pneumoniae, Staphylococcus spp., or H. influenzae.
Gonorrhea, acute uncomplicated (ano-genital and urethral infections) - due to N. gonorrhoeae (males and females).
H. pylori eradication to reduce the risk of duodenal ulcer recurrence
Triple Therapy: Amoxicillin/clarithromycin/lansoprazole

Amoxicillin, in combination with clarithromycin plus lansoprazole as triple therapy, is indicated for the treatment of patients with H. pylori infection and duodenal ulcer disease (active or 1-year history of a duodenal ulcer) to eradicate H. pylori. Eradication of H. pylori has been shown to reduce the risk of duodenal ulcer recurrence.. Common adverse reactions include As with other penicillins, it may be expected that untoward reactions will be essentially limited to sensitivity phenomena. They are more likely to occur in individuals who have previously demonstrated hypersensitivity to penicillins and in those with a history of allergy, asthma, hay fever, or urticaria. The following adverse reactions have been reported as associated with the use of penicillins:

Infections and Infestations: Mucocutaneous candidiasis.
Gastrointestinal: Nausea, vomiting, diarrhea, black hairy tongue, and hemorrhagic/pseudomembranous colitis.
Onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment. (See WARNINGS.)
Hypersensitivity Reactions: Anaphylaxis (See WARNING)
Serum sickness-like reactions, erythematous maculopapular rashes, erythema multiforme, Stevens-Johnson syndrome, exfoliative dermatitis, toxic epidermal necrolysis, acute generalized exanthematous pustulosis, hypersensitivity vasculitis and urticaria have been reported.NOTE: These hypersensitivity reactions may be controlled with antihistamines and, if necessary, systemic corticosteroids. Whenever such reactions occur, amoxicillin should be discontinued unless, in the opinion of the physician, the condition being treated is life-threatening and amenable only to amoxicillin therapy.
Liver: A moderate rise in AST (SGOT) and/or ALT (SGPT) has been noted, but the significance of this finding is unknown. Hepatic dysfunction including cholestatic jaundice, hepatic cholestasis and acute cytolytic hepatitis have been reported.
Renal: Crystalluria has also been reported (see OVERDOSAGE).
Hemic and Lymphatic Systems: Anemia, including hemolytic anemia, thrombocytopenia, thrombocytopenic purpura, eosinophilia, leukopenia, and agranulocytosis have been reported during therapy with penicillins. These reactions are usually reversible on discontinuation of therapy and are believed to be hypersensitivity phenomena.
Central Nervous System: Reversible hyperactivity, agitation, anxiety, insomnia, confusion, convulsions, behavioral changes, and/or dizziness have been reported rarely.
Miscellaneous: Tooth discoloration (brown, yellow, or gray staining) has been rarely reported. Most reports occurred in pediatric patients. Discoloration was reduced or eliminated with brushing or dental cleaning in most cases.
Combination Therapy with Clarithromycin and Lansoprazole: In clinical trials using combination therapy with amoxicillin plus clarithromycin and lansoprazole, and amoxicillin plus lansoprazole, no adverse reactions peculiar to these drug combinations were observed. Adverse reactions that have occurred have been limited to those that had been previously reported with amoxicillin, clarithromycin, or lansoprazole.
Triple Therapy: Amoxicillin/Clarithromycin/Lansoprazole:The most frequently reported adverse events for patients who received triple therapy were diarrhea (7%), headache (6%), and taste perversion (5%). No treatment-emergent adverse events were observed at significantly higher rates with triple therapy than with any dual therapy regimen.
Dual Therapy: Amoxicillin/Lansoprazole: The most frequently reported adverse events for patients who received amoxicillin three times daily plus lansoprazole three times daily dual therapy were diarrhea (8%) and headache (7%). No treatment-emergent adverse events were observed at significantly higher rates with amoxicillin three times daily plus lansoprazole three times daily dual therapy than with lansoprazole alone.

For more information on adverse reactions with clarithromycin or lansoprazole, refer to their package inserts, ADVERSE REACTIONS..

Adult Indications and Dosage

FDA-Labeled Indications and Dosage (Adult)

There is limited information regarding Amoxicillin FDA-Labeled Indications and Dosage (Adult) in the drug label.

Off-Label Use and Dosage (Adult)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Amoxicillin in adult patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Amoxicillin in adult patients.

Pediatric Indications and Dosage

FDA-Labeled Indications and Dosage (Pediatric)

There is limited information regarding Amoxicillin FDA-Labeled Indications and Dosage (Pediatric) in the drug label.

Off-Label Use and Dosage (Pediatric)

Guideline-Supported Use

There is limited information regarding Off-Label Guideline-Supported Use of Amoxicillin in pediatric patients.

Non–Guideline-Supported Use

There is limited information regarding Off-Label Non–Guideline-Supported Use of Amoxicillin in pediatric patients.

Contraindications

There is limited information regarding Amoxicillin Contraindications in the drug label.

Warnings

There is limited information regarding Amoxicillin Warnings' in the drug label.

Adverse Reactions

Clinical Trials Experience

There is limited information regarding Amoxicillin Clinical Trials Experience in the drug label.

Postmarketing Experience

There is limited information regarding Amoxicillin Postmarketing Experience in the drug label.

Drug Interactions

There is limited information regarding Amoxicillin Drug Interactions in the drug label.

Use in Specific Populations

Pregnancy

Pregnancy Category (FDA): There is no FDA guidance on usage of Amoxicillin in women who are pregnant.
Pregnancy Category (AUS): There is no Australian Drug Evaluation Committee (ADEC) guidance on usage of Amoxicillin in women who are pregnant.

Labor and Delivery

There is no FDA guidance on use of Amoxicillin during labor and delivery.

Nursing Mothers

There is no FDA guidance on the use of Amoxicillin in women who are nursing.

Pediatric Use

There is no FDA guidance on the use of Amoxicillin in pediatric settings.

Geriatic Use

There is no FDA guidance on the use of Amoxicillin in geriatric settings.

Gender

There is no FDA guidance on the use of Amoxicillin with respect to specific gender populations.

Race

There is no FDA guidance on the use of Amoxicillin with respect to specific racial populations.

Renal Impairment

There is no FDA guidance on the use of Amoxicillin in patients with renal impairment.

Hepatic Impairment

There is no FDA guidance on the use of Amoxicillin in patients with hepatic impairment.

Females of Reproductive Potential and Males

There is no FDA guidance on the use of Amoxicillin in women of reproductive potentials and males.

Immunocompromised Patients

There is no FDA guidance one the use of Amoxicillin in patients who are immunocompromised.

Administration and Monitoring

Administration

There is limited information regarding Amoxicillin Administration in the drug label.

Monitoring

There is limited information regarding Amoxicillin Monitoring in the drug label.

IV Compatibility

There is limited information regarding the compatibility of Amoxicillin and IV administrations.

Overdosage

There is limited information regarding Amoxicillin overdosage. If you suspect drug poisoning or overdose, please contact the National Poison Help hotline (1-800-222-1222) immediately.

Pharmacology

There is limited information regarding Amoxicillin Pharmacology in the drug label.

Mechanism of Action

There is limited information regarding Amoxicillin Mechanism of Action in the drug label.

Structure

There is limited information regarding Amoxicillin Structure in the drug label.

Pharmacodynamics

There is limited information regarding Amoxicillin Pharmacodynamics in the drug label.

Pharmacokinetics

There is limited information regarding Amoxicillin Pharmacokinetics in the drug label.

Nonclinical Toxicology

There is limited information regarding Amoxicillin Nonclinical Toxicology in the drug label.

Clinical Studies

There is limited information regarding Amoxicillin Clinical Studies in the drug label.

How Supplied

There is limited information regarding Amoxicillin How Supplied in the drug label.

Storage

There is limited information regarding Amoxicillin Storage in the drug label.

Images

Drug Images

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Package and Label Display Panel

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Patient Counseling Information

There is limited information regarding Amoxicillin Patient Counseling Information in the drug label.

Precautions with Alcohol

Alcohol-Amoxicillin interaction has not been established. Talk to your doctor about the effects of taking alcohol with this medication.

Brand Names

There is limited information regarding Amoxicillin Brand Names in the drug label.

Look-Alike Drug Names

There is limited information regarding Amoxicillin Look-Alike Drug Names in the drug label.

Drug Shortage Status

Price

References

The contents of this FDA label are provided by the National Library of Medicine.

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Amoxicillin
MOXATAG^® FDA Package Insert
Description
Clinical Pharmacology
Microbiology
Indications and Usage
Contraindications
Warnings and Precautions
Adverse Reactions
Overdosage
Dosage and Administration
How Supplied

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [2]; Associate Editor(s)-in-Chief: Mohamed Moubarak, M.D. [3]

Overview

Amoxicillin (INN), formerly amoxycillin (BAN), and abbreviated amox, is a moderate-spectrum, bacteriolytic, β-lactam antibiotic used to treat bacterial infections caused by susceptible microorganisms. It is usually the drug of choice within the class because it is better absorbed, following oral administration, than other β-lactam antibiotics. Amoxicillin is one of the most common antibiotics prescribed for children. The drug first became available in 1972.

Amoxicillin is susceptible to degradation by β-lactamase-producing bacteria, which are resistant to a broad spectrum of β-lactam antibiotics, such as penicillin. For this reason, it is often combined with clavulanic acid, a β-lactamase inhibitor. This increases effectiveness by reducing its susceptibility to β-lactamase resistance.^[1]

US Brand Names

MOXATAG^®

FDA Package Insert

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Mechanism of Action

Amoxicillin is similar to ampicillin in its bactericidal action against susceptible organisms during the stage of active multiplication. It acts through the inhibition of biosynthesis of cell wall mucopeptide.

References

↑ "Amoxicillin Susceptibility and Resistance Data" (PDF). Text "accessdate" ignored (help)

[1] "Amoxicillin Susceptibility and Resistance Data" (PDF). Text "accessdate" ignored (help)

[1]

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+|indication=Amoxicillin is indicated in the treatment of infections due to susceptible (ONLY β-lactamase-negative) strains of the designated microorganisms in the conditions listed below:
+*Infections of the ear, nose, and throat - due to Streptococcus spp. (α- and β-hemolytic strains only), S. pneumoniae, Staphylococcus spp., or H. influenzae.
+*Infections of the genitourinary tract - due to E. coli, P. mirabilis, or E. faecalis.
+*Infections of the skin and skin structure - due to Streptococcus spp. (α- and β-hemolytic strains only), Staphylococcus spp., or E. coli.
+*Infections of the lower respiratory tract -due to Streptococcus spp. (α- and β-hemolytic strains only), S. pneumoniae, Staphylococcus spp., or H. influenzae.
+*Gonorrhea, acute uncomplicated (ano-genital and urethral infections) - due to N. gonorrhoeae (males and females).
+*H. pylori eradication to reduce the risk of duodenal ulcer recurrence
+*Triple Therapy: Amoxicillin/clarithromycin/lansoprazole
+Amoxicillin, in combination with clarithromycin plus lansoprazole as triple therapy, is indicated for the treatment of patients with H. pylori infection and duodenal ulcer disease (active or 1-year history of a duodenal ulcer) to eradicate H. pylori. Eradication of H. pylori has been shown to reduce the risk of duodenal ulcer recurrence.
+|adverseReactions=As with other penicillins, it may be expected that untoward reactions will be essentially limited to sensitivity phenomena. They are more likely to occur in individuals who have previously demonstrated hypersensitivity to penicillins and in those with a history of allergy, asthma, hay fever, or urticaria. The following adverse reactions have been reported as associated with the use of penicillins:
+*Infections and Infestations: Mucocutaneous candidiasis.
+*Gastrointestinal: Nausea, vomiting, diarrhea, black hairy tongue, and hemorrhagic/pseudomembranous colitis.
+*Onset of pseudomembranous colitis symptoms may occur during or after antibiotic treatment. (See WARNINGS.)
+*Hypersensitivity Reactions: Anaphylaxis (See WARNING)
+*Serum sickness-like reactions, erythematous maculopapular rashes, erythema multiforme, Stevens-Johnson syndrome, exfoliative dermatitis, toxic epidermal necrolysis, acute generalized exanthematous pustulosis, hypersensitivity vasculitis and urticaria have been reported.NOTE: These hypersensitivity reactions may be controlled with antihistamines and, if necessary, systemic corticosteroids. Whenever such reactions occur, amoxicillin should be discontinued unless, in the opinion of the physician, the condition being treated is life-threatening and amenable only to amoxicillin therapy.
+*Liver: A moderate rise in AST (SGOT) and/or ALT (SGPT) has been noted, but the significance of this finding is unknown. Hepatic dysfunction including cholestatic jaundice, hepatic cholestasis and acute cytolytic hepatitis have been reported.
+*Renal: Crystalluria has also been reported (see OVERDOSAGE).
+*Hemic and Lymphatic Systems: Anemia, including hemolytic anemia, thrombocytopenia, thrombocytopenic purpura, eosinophilia, leukopenia, and agranulocytosis have been reported during therapy with penicillins. These reactions are usually reversible on discontinuation of therapy and are believed to be hypersensitivity phenomena.
+*Central Nervous System: Reversible hyperactivity, agitation, anxiety, insomnia, confusion, convulsions, behavioral changes, and/or dizziness have been reported rarely.
+*Miscellaneous: Tooth discoloration (brown, yellow, or gray staining) has been rarely reported. Most reports occurred in pediatric patients. Discoloration was reduced or eliminated with brushing or dental cleaning in most cases.
+*Combination Therapy with Clarithromycin and Lansoprazole: In clinical trials using combination therapy with amoxicillin plus clarithromycin and lansoprazole, and amoxicillin plus lansoprazole, no adverse reactions peculiar to these drug combinations were observed. Adverse reactions that have occurred have been limited to those that had been previously reported with amoxicillin, clarithromycin, or lansoprazole.
+*Triple Therapy: Amoxicillin/Clarithromycin/Lansoprazole:The most frequently reported adverse events for patients who received triple therapy were diarrhea (7%), headache (6%), and taste perversion (5%). No treatment-emergent adverse events were observed at significantly higher rates with triple therapy than with any dual therapy regimen.
+*Dual Therapy: Amoxicillin/Lansoprazole: The most frequently reported adverse events for patients who received amoxicillin three times daily plus lansoprazole three times daily dual therapy were diarrhea (8%) and headache (7%). No treatment-emergent adverse events were observed at significantly higher rates with amoxicillin three times daily plus lansoprazole three times daily dual therapy than with lansoprazole alone.
+For more information on adverse reactions with clarithromycin or lansoprazole, refer to their package inserts, ADVERSE REACTIONS.
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 {{Amoxicillin}}
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-{{PillImage|fileName=Amoxicillin_NDC_00932268.jpg|drugName=Amoxicillin|NDC=00932268|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=9;3;2268|dosageValue=250|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=19|pillScore=2}}
-{{PillImage|fileName=Amoxicillin_NDC_00933107.jpg|drugName=Amoxicillin|NDC=00933107|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=TEVA;3107|dosageValue=250|dosageUnit=mg|pillColor=Brown;Brown|pillShape=Capsule|pillSize=18|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_NDC_00933109.jpg|drugName=Amoxicillin|NDC=00933109|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=TEVA;3109|dosageValue=500|dosageUnit=mg|pillColor=Brown|pillShape=Capsule|pillSize=22|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_NDC_597621020.jpg|drugName=Amoxicillin|NDC=597621020|drugAuthor=Greenstone LLC|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=A44|dosageValue=250|dosageUnit=mg|pillColor=Blue;Pink|pillShape=Capsule|pillSize=19|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_NDC_597621050.jpg|drugName=Amoxicillin|NDC=597621050|drugAuthor=Greenstone LLC|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=A;6;7|dosageValue=875|dosageUnit=mg|pillColor=Pink|pillShape=Oval|pillSize=21|pillScore=2}}
-{{PillImage|fileName=Amoxicillin_NDC_552890020.jpg|drugName=Amoxicillin|NDC=552890020|drugAuthor=PD-Rx Pharmaceuticals, Inc.|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=TEVA;3109|dosageValue=500|dosageUnit=ug|pillColor=Brown|pillShape=Capsule|pillSize=22|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_NDC_658620017.jpg|drugName=Amoxicillin|NDC=658620017|drugAuthor=Aurobindo Pharma Limited|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=A45|dosageValue=500|dosageUnit=mg|pillColor=Blue;Pink|pillShape=Capsule|pillSize=23|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_NDC_672530141.jpg|drugName=Amoxicillin|NDC=672530141|drugAuthor=DAVA Pharmaceuticals, Inc.|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=WC;731|dosageValue=500|dosageUnit=mg|pillColor=Orange;Red;Pink|pillShape=Capsule|pillSize=23|pillScore=1}}
-{{PillImage|fileName=Moxatag_NDC_684530142.jpg|drugName=Moxatag|NDC=684530142|drugAuthor=Victory Pharma, Inc. |ingredients=amoxicillin[amoxicillin]|pillImprint=MB;111|dosageValue=775|dosageUnit=mg|pillColor=Blue|pillShape=Oval|pillSize=22|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_NDC_430630434.jpg|drugName=Amoxicillin|NDC=430630434|drugAuthor=PD-Rx Pharmaceuticals, Inc.|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS]|pillImprint=TEVA;3109|dosageValue=500|dosageUnit=mg|pillColor=Brown|pillShape=Capsule|pillSize=22|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_00932270.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=00932270|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=93;2270|dosageValue=200|dosageUnit=mg|pillColor=Pink|pillShape=Oval|pillSize=16|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_00932272.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=00932272|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=93;2272|dosageValue=400|dosageUnit=mg|pillColor=Pink|pillShape=Oval|pillSize=21|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_00932274.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=00932274|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=93;2274|dosageValue=500|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=20|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_00932275.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=00932275|drugAuthor=Teva Pharmaceuticals USA Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=93;22;75|dosageValue=875|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=22|pillScore=2}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_07811874.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=07811874|drugAuthor=Sandoz Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=GGN5|dosageValue=250|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=18|pillScore=1}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_07811874.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=07811874|drugAuthor=Sandoz Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=GGN5|dosageValue=250|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=18|pillScore=1}}
-{{PillImage|fileName=AUGMENTIN_NDC_435980020.jpg|drugName=AUGMENTIN|NDC=435980020|drugAuthor=Dr Reddys Laboratories Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];AMOXICILLIN SODIUM[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=AUGMENTIN;XR|dosageValue=562.5|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=22|pillScore=2}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_435980220.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=435980220|drugAuthor=Dr Reddys Laboratories Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];AMOXICILLIN SODIUM[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=AUGMENTIN;XR|dosageValue=562.5|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=22|pillScore=2}}
-{{PillImage|fileName=Amoxicillin_and_Clavulanate_Potassium_NDC_07811943.jpg|drugName=Amoxicillin and Clavulanate Potassium|NDC=07811943|drugAuthor=Sandoz Inc|ingredients=AMOXICILLIN[AMOXICILLIN ANHYDROUS];AMOXICILLIN SODIUM[AMOXICILLIN ANHYDROUS];CLAVULANATE POTASSIUM[CLAVULANIC ACID]|pillImprint=SZ137|dosageValue=562.5|dosageUnit=mg|pillColor=White|pillShape=Oval|pillSize=22|pillScore=2}}
-{{PillImage|fileName=MOXATAG_NDC_110420142.jpg|drugName=MOXATAG|NDC=110420142|drugAuthor=MiddleBrook Pharmaceuticals, Inc.|ingredients=amoxicillin[amoxicillin]|pillImprint=MB-111|dosageValue=775|dosageUnit=mg|pillColor=Blue|pillShape=Oval|pillSize=22|pillScore=1}}
 ==Mechanism of Action==

Amoxicillin: Difference between revisions

Revision as of 14:17, 16 December 2014

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Overview

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