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Ciprofloxacin Hydrochloride - 49349-612-03 - (Ciprofloxacin Hydrochloride)

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Drug Information of Ciprofloxacin Hydrochloride

Product NDC: 49349-612
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin Hydrochloride

Product NDC: 49349-612
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075593
Marketing Category: ANDA
Start Marketing Date: 20110315

Package Information of Ciprofloxacin Hydrochloride

Package NDC: 49349-612-03
Package Description: 20 TABLET, FILM COATED in 1 BLISTER PACK (49349-612-03)

NDC Information of Ciprofloxacin Hydrochloride

NDC Code 49349-612-03
Proprietary Name Ciprofloxacin Hydrochloride
Package Description 20 TABLET, FILM COATED in 1 BLISTER PACK (49349-612-03)
Product NDC 49349-612
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110315
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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