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Ciprofloxacin - 55111-422-30 - (ciprofloxacin hydrochloride)

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Drug Information of Ciprofloxacin

Product NDC: 55111-422
Proprietary Name: Ciprofloxacin
Non Proprietary Name: ciprofloxacin hydrochloride
Active Ingredient(s): 212.6; 287.5    mg/1; mg/1 & nbsp;   ciprofloxacin hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Ciprofloxacin

Product NDC: 55111-422
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077902
Marketing Category: ANDA
Start Marketing Date: 20070326

Package Information of Ciprofloxacin

Package NDC: 55111-422-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-422-30)

NDC Information of Ciprofloxacin

NDC Code 55111-422-30
Proprietary Name Ciprofloxacin
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (55111-422-30)
Product NDC 55111-422
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ciprofloxacin hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070326
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name CIPROFLOXACIN; CIPROFLOXACIN HYDROCHLORIDE
Strength Number 212.6; 287.5
Strength Unit mg/1; mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient],Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ciprofloxacin


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