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ciprofloxacin - 43063-410-12 - (ciprofloxacin)

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Drug Information of ciprofloxacin

Product NDC: 43063-410
Proprietary Name: ciprofloxacin
Non Proprietary Name: ciprofloxacin
Active Ingredient(s): 250    mg/1 & nbsp;   ciprofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of ciprofloxacin

Product NDC: 43063-410
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076639
Marketing Category: ANDA
Start Marketing Date: 20040910

Package Information of ciprofloxacin

Package NDC: 43063-410-12
Package Description: 12 TABLET in 1 BOTTLE, PLASTIC (43063-410-12)

NDC Information of ciprofloxacin

NDC Code 43063-410-12
Proprietary Name ciprofloxacin
Package Description 12 TABLET in 1 BOTTLE, PLASTIC (43063-410-12)
Product NDC 43063-410
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040910
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
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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