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Ciprofloxacin - 51079-403-20 - (ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 51079-403
Proprietary Name: Ciprofloxacin
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 Ciprofloxacin

Product NDC: 51079-403
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075685
Marketing Category: ANDA
Start Marketing Date: 20110628

Package Information of Ciprofloxacin

Package NDC: 51079-403-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-403-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-403-01)

NDC Information of Ciprofloxacin

NDC Code 51079-403-20
Proprietary Name Ciprofloxacin
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-403-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-403-01)
Product NDC 51079-403
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110628
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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