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Ciprofloxacin - 63739-559-10 - (Ciprofloxacin Hydrochloride)

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Drug Information of Ciprofloxacin

Product NDC: 63739-559
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin Hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 63739-559
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077859
Marketing Category: ANDA
Start Marketing Date: 20121120

Package Information of Ciprofloxacin

Package NDC: 63739-559-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-559-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Ciprofloxacin

NDC Code 63739-559-10
Proprietary Name Ciprofloxacin
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-559-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-559
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20121120
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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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