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Ciprofloxacin - 21695-411-10 - (ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin

Product NDC: 21695-411
Proprietary Name: Ciprofloxacin
Non Proprietary Name: ciprofloxacin hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   ciprofloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 21695-411
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076794
Marketing Category: ANDA
Start Marketing Date: 20030819

Package Information of Ciprofloxacin

Package NDC: 21695-411-10
Package Description: 10 TABLET in 1 BOTTLE (21695-411-10)

NDC Information of Ciprofloxacin

NDC Code 21695-411-10
Proprietary Name Ciprofloxacin
Package Description 10 TABLET in 1 BOTTLE (21695-411-10)
Product NDC 21695-411
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030819
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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