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Ciprofloxacin - 60505-1308-2 - (ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin

Product NDC: 60505-1308
Proprietary Name: Ciprofloxacin
Non Proprietary Name: ciprofloxacin hydrochloride
Active Ingredient(s): 250    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

Product NDC: 60505-1308
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076896
Marketing Category: ANDA
Start Marketing Date: 20050419

Package Information of Ciprofloxacin

Package NDC: 60505-1308-2
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60505-1308-2)

NDC Information of Ciprofloxacin

NDC Code 60505-1308-2
Proprietary Name Ciprofloxacin
Package Description 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60505-1308-2)
Product NDC 60505-1308
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050419
Marketing Category Name ANDA
Labeler Name Apotex Corp
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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