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Ciprofloxacin hydrochloride - 0179-1982-14 - (Ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin hydrochloride

Product NDC: 0179-1982
Proprietary Name: Ciprofloxacin hydrochloride
Non Proprietary Name: Ciprofloxacin hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin hydrochloride

Product NDC: 0179-1982
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076089
Marketing Category: ANDA
Start Marketing Date: 20110623

Package Information of Ciprofloxacin hydrochloride

Package NDC: 0179-1982-14
Package Description: 14 TABLET in 1 BOTTLE (0179-1982-14)

NDC Information of Ciprofloxacin hydrochloride

NDC Code 0179-1982-14
Proprietary Name Ciprofloxacin hydrochloride
Package Description 14 TABLET in 1 BOTTLE (0179-1982-14)
Product NDC 0179-1982
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110623
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin hydrochloride


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