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Ciprofloxacin - 21695-210-06 - (ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin

Product NDC: 21695-210
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: 21695-210
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076794
Marketing Category: ANDA
Start Marketing Date: 20040609

Package Information of Ciprofloxacin

Package NDC: 21695-210-06
Package Description: 6 TABLET, FILM COATED in 1 BOTTLE (21695-210-06)

NDC Information of Ciprofloxacin

NDC Code 21695-210-06
Proprietary Name Ciprofloxacin
Package Description 6 TABLET, FILM COATED in 1 BOTTLE (21695-210-06)
Product NDC 21695-210
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 Rebel Distributors Corp.
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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