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Ciprofloxacin - 52125-069-02 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 52125-069
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 52125-069
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076558
Marketing Category: ANDA
Start Marketing Date: 20130314

Package Information of Ciprofloxacin

Package NDC: 52125-069-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-069-02)

NDC Information of Ciprofloxacin

NDC Code 52125-069-02
Proprietary Name Ciprofloxacin
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (52125-069-02)
Product NDC 52125-069
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130314
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


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