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CIPROFLOXACIN HYDROCHLORIDE - 67296-0543-2 - (ciprofloxacin hydrochloride tablet)

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Drug Information of CIPROFLOXACIN HYDROCHLORIDE

Product NDC: 67296-0543
Proprietary Name: CIPROFLOXACIN HYDROCHLORIDE
Non Proprietary Name: ciprofloxacin hydrochloride tablet
Active Ingredient(s): 500    mg/1 & nbsp;   ciprofloxacin hydrochloride tablet
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CIPROFLOXACIN HYDROCHLORIDE

Product NDC: 67296-0543
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076089
Marketing Category: ANDA
Start Marketing Date: 20110404

Package Information of CIPROFLOXACIN HYDROCHLORIDE

Package NDC: 67296-0543-2
Package Description: 10 TABLET in 1 BOTTLE (67296-0543-2)

NDC Information of CIPROFLOXACIN HYDROCHLORIDE

NDC Code 67296-0543-2
Proprietary Name CIPROFLOXACIN HYDROCHLORIDE
Package Description 10 TABLET in 1 BOTTLE (67296-0543-2)
Product NDC 67296-0543
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride tablet
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110404
Marketing Category Name ANDA
Labeler Name RedPharm Drug 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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