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Ciprofloxacin Hydrochloride - 49349-854-01 - (Ciprofloxacin Hydrochloride)

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Drug Information of Ciprofloxacin Hydrochloride

Product NDC: 49349-854
Proprietary Name: Ciprofloxacin Hydrochloride
Non Proprietary Name: Ciprofloxacin Hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin Hydrochloride

Product NDC: 49349-854
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076639
Marketing Category: ANDA
Start Marketing Date: 20111212

Package Information of Ciprofloxacin Hydrochloride

Package NDC: 49349-854-01
Package Description: 1 TABLET in 1 VIAL (49349-854-01)

NDC Information of Ciprofloxacin Hydrochloride

NDC Code 49349-854-01
Proprietary Name Ciprofloxacin Hydrochloride
Package Description 1 TABLET in 1 VIAL (49349-854-01)
Product NDC 49349-854
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111212
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin Hydrochloride


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