Cipro - 0085-1741-02 - (ciprofloxacin)

Alphabetical Index


Drug Information of Cipro

Product NDC: 0085-1741
Proprietary Name: Cipro
Non Proprietary Name: ciprofloxacin
Active Ingredient(s): 2    mg/mL & nbsp;   ciprofloxacin
Administration Route(s): INTRAVENOUS
Dosage Form(s): SOLUTION, CONCENTRATE
Coding System: National Drug Codes(NDC)

Labeler Information of Cipro

Product NDC: 0085-1741
Labeler Name: Schering Plough Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019857
Marketing Category: NDA
Start Marketing Date: 20090427

Package Information of Cipro

Package NDC: 0085-1741-02
Package Description: 200 mL in 1 BOTTLE, PLASTIC (0085-1741-02)

NDC Information of Cipro

NDC Code 0085-1741-02
Proprietary Name Cipro
Package Description 200 mL in 1 BOTTLE, PLASTIC (0085-1741-02)
Product NDC 0085-1741
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name SOLUTION, CONCENTRATE
Route Name INTRAVENOUS
Start Marketing Date 20090427
Marketing Category Name NDA
Labeler Name Schering Plough Corporation
Substance Name CIPROFLOXACIN
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Cipro


General Information