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Ciprofloxacin - 61442-224-04 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 61442-224
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 750    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: 61442-224
Labeler Name: Carlsbad Technology, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076126
Marketing Category: ANDA
Start Marketing Date: 20091010

Package Information of Ciprofloxacin

Package NDC: 61442-224-04
Package Description: 400 TABLET, FILM COATED in 1 BOTTLE (61442-224-04)

NDC Information of Ciprofloxacin

NDC Code 61442-224-04
Proprietary Name Ciprofloxacin
Package Description 400 TABLET, FILM COATED in 1 BOTTLE (61442-224-04)
Product NDC 61442-224
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20091010
Marketing Category Name ANDA
Labeler Name Carlsbad Technology, Inc.
Substance Name CIPROFLOXACIN HYDROCHLORIDE
Strength Number 750
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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