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Ciprofloxacin - 10544-608-20 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 10544-608
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 10544-608
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076639
Marketing Category: ANDA
Start Marketing Date: 20100517

Package Information of Ciprofloxacin

Package NDC: 10544-608-20
Package Description: 20 TABLET in 1 BOTTLE (10544-608-20)

NDC Information of Ciprofloxacin

NDC Code 10544-608-20
Proprietary Name Ciprofloxacin
Package Description 20 TABLET in 1 BOTTLE (10544-608-20)
Product NDC 10544-608
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100517
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
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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