Proquin - 13913-001-91 - (ciprofloxacin hydrochloride)

Alphabetical Index


Drug Information of Proquin

Product NDC: 13913-001
Proprietary Name: Proquin
Non Proprietary Name: ciprofloxacin hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   ciprofloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Proquin

Product NDC: 13913-001
Labeler Name: Depomed, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021744
Marketing Category: NDA
Start Marketing Date: 20051001

Package Information of Proquin

Package NDC: 13913-001-91
Package Description: 1 BLISTER PACK in 1 CARTON (13913-001-91) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Proquin

NDC Code 13913-001-91
Proprietary Name Proquin
Package Description 1 BLISTER PACK in 1 CARTON (13913-001-91) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 13913-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20051001
Marketing Category Name NDA
Labeler Name Depomed, Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Proquin


General Information