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Ciprofloxacin - 63304-710-80 - (Ciprofloxacin)

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Drug Information of Ciprofloxacin

Product NDC: 63304-710
Proprietary Name: Ciprofloxacin
Non Proprietary Name: Ciprofloxacin
Active Ingredient(s): 500    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: 63304-710
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075747
Marketing Category: ANDA
Start Marketing Date: 20040609

Package Information of Ciprofloxacin

Package NDC: 63304-710-80
Package Description: 100 TABLET, FILM COATED in 1 BLISTER PACK (63304-710-80)

NDC Information of Ciprofloxacin

NDC Code 63304-710-80
Proprietary Name Ciprofloxacin
Package Description 100 TABLET, FILM COATED in 1 BLISTER PACK (63304-710-80)
Product NDC 63304-710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ciprofloxacin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20040609
Marketing Category Name ANDA
Labeler Name Ranbaxy 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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