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Ciprofloxacin - 24658-250-05 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 24658-250
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 24658-250
Labeler Name: Blu Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076558
Marketing Category: ANDA
Start Marketing Date: 20040609

Package Information of Ciprofloxacin

Package NDC: 24658-250-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (24658-250-05)

NDC Information of Ciprofloxacin

NDC Code 24658-250-05
Proprietary Name Ciprofloxacin
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (24658-250-05)
Product NDC 24658-250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040609
Marketing Category Name ANDA
Labeler Name Blu Pharmaceuticals, LLC
Substance Name CIPROFLOXACIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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