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Ciprofloxacin - 51079-181-20 - (ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 51079-181
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: 51079-181
Labeler Name: Mylan Institutional Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075817
Marketing Category: ANDA
Start Marketing Date: 20120629

Package Information of Ciprofloxacin

Package NDC: 51079-181-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-181-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-181-01)

NDC Information of Ciprofloxacin

NDC Code 51079-181-20
Proprietary Name Ciprofloxacin
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-181-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-181-01)
Product NDC 51079-181
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120629
Marketing Category Name ANDA
Labeler Name Mylan Institutional 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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