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Ciprofloxacin - 52959-734-30 - (ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin

Product NDC: 52959-734
Proprietary Name: Ciprofloxacin
Non Proprietary Name: ciprofloxacin hydrochloride
Active Ingredient(s): 750    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: 52959-734
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076794
Marketing Category: ANDA
Start Marketing Date: 20040609

Package Information of Ciprofloxacin

Package NDC: 52959-734-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-734-30)

NDC Information of Ciprofloxacin

NDC Code 52959-734-30
Proprietary Name Ciprofloxacin
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-734-30)
Product NDC 52959-734
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040609
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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