Mexiletine how supplied storage and handling: Difference between revisions
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==How Supplied Storage And Handling== | ==How Supplied Storage And Handling== |
Revision as of 15:56, 10 March 2014
Mexiletine |
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MEXILETINE HYDROCHLORIDE® FDA Package Insert |
Indications and Usage |
Dosage and Administration |
Contraindications |
Warnings and Precautions |
Adverse Reactions |
Drug Interactions |
Use in Specific Populations |
Overdosage |
Description |
Clinical Pharmacology |
How Supplied/Storage and Handling |
Labels and Packages |
Clinical Trials on Mexiletine |
ClinicalTrials.gov |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Sheng Shi, M.D. [2]; Ahmed Zaghw, M.D. [3]
How Supplied Storage And Handling
Mexiletine hydrochloride capsules USP, 150 mg are white granular powder in a hard gelatin capsule with an opaque tan cap and an opaque orange body, imprinted with "N" on one side and "739" and "150" on the other in black ink. They are supplied as follows: NDC 0093-8739-01 bottles of 100.
Mexiletine hydrochloride capsules USP, 200 mg are white granular powder in a hard gelatin capsule with an opaque orange cap and an opaque orange body, imprinted with "N" on one side and "740" and "200" on the other in black ink. They are supplied as follows: NDC 0093-8740-01 bottles of 100.
Mexiletine hydrochloride capsules USP, 250 mg are white granular powder in a hard gelatin capsule with an opaque green cap and an opaque orange body, imprinted with "N" on one side and "741" and "250" on the other in black ink. They are supplied as follows: NDC 0093-8741-01 bottles of 100.
Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required)..[1]
References
- ↑ "MEXILETINE HYDROCHLORIDE CAPSULE [TEVA PHARMACEUTICALS USA INC]". Retrieved 3 March 2014.