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Ciprofloxacin hydrochloride - 10544-606-14 - (Ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin hydrochloride

Product NDC: 10544-606
Proprietary Name: Ciprofloxacin hydrochloride
Non Proprietary Name: Ciprofloxacin hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   Ciprofloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin hydrochloride

Product NDC: 10544-606
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076089
Marketing Category: ANDA
Start Marketing Date: 20100517

Package Information of Ciprofloxacin hydrochloride

Package NDC: 10544-606-14
Package Description: 14 TABLET in 1 BOTTLE (10544-606-14)

NDC Information of Ciprofloxacin hydrochloride

NDC Code 10544-606-14
Proprietary Name Ciprofloxacin hydrochloride
Package Description 14 TABLET in 1 BOTTLE (10544-606-14)
Product NDC 10544-606
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin hydrochloride
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 hydrochloride


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