Cipro - 50419-758-01 - (ciprofloxacin hydrochloride)

Alphabetical Index


Drug Information of Cipro

Product NDC: 50419-758
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: 50419-758
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019537
Marketing Category: NDA
Start Marketing Date: 19871022

Package Information of Cipro

Package NDC: 50419-758-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-758-01)

NDC Information of Cipro

NDC Code 50419-758-01
Proprietary Name Cipro
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-758-01)
Product NDC 50419-758
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19871022
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals 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