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Ciprofloxacin - 13107-076-30 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 13107-076
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 250    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: 13107-076
Labeler Name: Aurolife Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077859
Marketing Category: ANDA
Start Marketing Date: 20090801

Package Information of Ciprofloxacin

Package NDC: 13107-076-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (13107-076-30)

NDC Information of Ciprofloxacin

NDC Code 13107-076-30
Proprietary Name Ciprofloxacin
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (13107-076-30)
Product NDC 13107-076
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090801
Marketing Category Name ANDA
Labeler Name Aurolife Pharma LLC
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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