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Ciprofloxacin - 49349-662-02 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 49349-662
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 250    mg/1 & nbsp;   Ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 49349-662
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076794
Marketing Category: ANDA
Start Marketing Date: 20110523

Package Information of Ciprofloxacin

Package NDC: 49349-662-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-662-02)

NDC Information of Ciprofloxacin

NDC Code 49349-662-02
Proprietary Name Ciprofloxacin
Package Description 30 TABLET in 1 BLISTER PACK (49349-662-02)
Product NDC 49349-662
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110523
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


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