Cipro - 0085-1775-01 - (ciprofloxacin)

Alphabetical Index


Drug Information of Cipro

Product NDC: 0085-1775
Proprietary Name: Cipro
Non Proprietary Name: ciprofloxacin
Active Ingredient(s): 500    mg/1 & nbsp;   ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cipro

Product NDC: 0085-1775
Labeler Name: Schering Plough Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021473
Marketing Category: NDA
Start Marketing Date: 20090427

Package Information of Cipro

Package NDC: 0085-1775-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0085-1775-01)

NDC Information of Cipro

NDC Code 0085-1775-01
Proprietary Name Cipro
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0085-1775-01)
Product NDC 0085-1775
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090427
Marketing Category Name NDA
Labeler Name Schering Plough Corporation
Substance Name CIPROFLOXACIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Cipro


General Information