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ciprofloxacin - 68788-9012-1 - (ciprofloxacin)

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Drug Information of ciprofloxacin

Product NDC: 68788-9012
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: 68788-9012
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076639
Marketing Category: ANDA
Start Marketing Date: 20110609

Package Information of ciprofloxacin

Package NDC: 68788-9012-1
Package Description: 14 TABLET in 1 BOTTLE (68788-9012-1)

NDC Information of ciprofloxacin

NDC Code 68788-9012-1
Proprietary Name ciprofloxacin
Package Description 14 TABLET in 1 BOTTLE (68788-9012-1)
Product NDC 68788-9012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110609
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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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