Home > National Drug Code (NDC) > Ciprofloxacin

Ciprofloxacin - 62037-938-01 - (Ciprofloxacin)

Alphabetical Index


Drug Information of Ciprofloxacin

Product NDC: 62037-938
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 425.2; 574.9    mg/1; mg/1 & nbsp;   Ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 62037-938
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077809
Marketing Category: ANDA
Start Marketing Date: 20101130

Package Information of Ciprofloxacin

Package NDC: 62037-938-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-938-01)

NDC Information of Ciprofloxacin

NDC Code 62037-938-01
Proprietary Name Ciprofloxacin
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-938-01)
Product NDC 62037-938
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20101130
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Strength Number 425.2; 574.9
Strength Unit mg/1; mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


General Information