Home > National Drug Code (NDC) > Ciprofloxacin

Ciprofloxacin - 65862-077-99 - (Ciprofloxacin Hydrochloride)

Alphabetical Index


Drug Information of Ciprofloxacin

Product NDC: 65862-077
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin Hydrochloride
Active Ingredient(s): 500    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: 65862-077
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077859
Marketing Category: ANDA
Start Marketing Date: 20070426

Package Information of Ciprofloxacin

Package NDC: 65862-077-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-077-99)

NDC Information of Ciprofloxacin

NDC Code 65862-077-99
Proprietary Name Ciprofloxacin
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (65862-077-99)
Product NDC 65862-077
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070426
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


General Information