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ciprofloxacin - 50436-3135-3 - (ciprofloxacin)

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Drug Information of ciprofloxacin

Product NDC: 50436-3135
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: 50436-3135
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076639
Marketing Category: ANDA
Start Marketing Date: 20040910

Package Information of ciprofloxacin

Package NDC: 50436-3135-3
Package Description: 21 TABLET in 1 BOTTLE (50436-3135-3)

NDC Information of ciprofloxacin

NDC Code 50436-3135-3
Proprietary Name ciprofloxacin
Package Description 21 TABLET in 1 BOTTLE (50436-3135-3)
Product NDC 50436-3135
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040910
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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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