Cipro - 50419-788-01 - (ciprofloxacin)

Alphabetical Index


Drug Information of Cipro

Product NDC: 50419-788
Proprietary Name: Cipro
Non Proprietary Name: ciprofloxacin
Active Ingredient(s): 212.6; 287.5    mg/1; 1/1 & nbsp;   ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Cipro

Product NDC: 50419-788
Labeler Name: Bayer HealthCare Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021473
Marketing Category: NDA
Start Marketing Date: 20121001

Package Information of Cipro

Package NDC: 50419-788-01
Package Description: 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50419-788-01)

NDC Information of Cipro

NDC Code 50419-788-01
Proprietary Name Cipro
Package Description 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50419-788-01)
Product NDC 50419-788
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20121001
Marketing Category Name NDA
Labeler Name Bayer HealthCare Pharmaceuticals Inc.
Substance Name CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Strength Number 212.6; 287.5
Strength Unit mg/1; 1/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Cipro


General Information