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Ciprofloxacin - 0378-1322-01 - (ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 0378-1322
Proprietary Name: Ciprofloxacin
Non Proprietary Name: ciprofloxacin
Active Ingredient(s): 250    mg/1 & nbsp;   ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 0378-1322
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075685
Marketing Category: ANDA
Start Marketing Date: 20120110

Package Information of Ciprofloxacin

Package NDC: 0378-1322-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1322-01)

NDC Information of Ciprofloxacin

NDC Code 0378-1322-01
Proprietary Name Ciprofloxacin
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1322-01)
Product NDC 0378-1322
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120110
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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