CARDENE I.V. labels and packaging: Difference between revisions
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|} | |}<ref> {{cite web | url = http://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f8ef8420-01d2-11de-a455-0002a5d5c51b | title = CARDENE I.V. (nicardipine hydrochloride) injection, solution [EKR Therapeutics, Inc.] |accessdate = }}</ref> | ||
==References== | |||
{{Reflist|2}} | {{Reflist|2}} | ||
{{FDA}} | |||
[[Category:Cardiovascular Drugs]] | [[Category:Cardiovascular Drugs]] | ||
[[Category:Drugs]] | [[Category:Drugs]] | ||
Revision as of 16:39, 20 February 2014
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: :Abdurahman Khalil, M.D. [2]
For patient information about Nicardipine, click here. Revised September 2010
CAR10-249
07-19-65-231
Package Label - Principal Display Panel - 0.2 mg (Dextrose diluent) Bag
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Package Label - Principal Display Panel - 0.2 mg (Dextrose diluent) Carton
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Package Label - Principal Display Panel - 0.2 mg (Sodium Chloride diluent) Bag
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Package Label - Principal Display Panel - 0.2 mg (Sodium Chloride diluent) Carton
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References
Adapted from the FDA Package Insert.