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Ciprofloxacin Hydrochloride - 49349-246-02 - (Ciprofloxacin Hydrochloride)

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Drug Information of Ciprofloxacin Hydrochloride

Product NDC: 49349-246
Proprietary Name: Ciprofloxacin Hydrochloride
Non Proprietary Name: Ciprofloxacin Hydrochloride
Active Ingredient(s): 250    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: 49349-246
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077859
Marketing Category: ANDA
Start Marketing Date: 20110505

Package Information of Ciprofloxacin Hydrochloride

Package NDC: 49349-246-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-246-02)

NDC Information of Ciprofloxacin Hydrochloride

NDC Code 49349-246-02
Proprietary Name Ciprofloxacin Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-246-02)
Product NDC 49349-246
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110505
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin Hydrochloride


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