Cipro - 54868-0990-0 - (ciprofloxacin hydrochloride)

Alphabetical Index


Drug Information of Cipro

Product NDC: 54868-0990
Proprietary Name: Cipro
Non Proprietary Name: ciprofloxacin hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   ciprofloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cipro

Product NDC: 54868-0990
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019537
Marketing Category: NDA
Start Marketing Date: 19950207

Package Information of Cipro

Package NDC: 54868-0990-0
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0990-0)

NDC Information of Cipro

NDC Code 54868-0990-0
Proprietary Name Cipro
Package Description 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0990-0)
Product NDC 54868-0990
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950207
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Cipro


General Information