Ofloxacin - 55111-162-78 - (ofloxacin)

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Drug Information of Ofloxacin

Product NDC: 55111-162
Proprietary Name: Ofloxacin
Non Proprietary Name: ofloxacin
Active Ingredient(s): 400    mg/1 & nbsp;   ofloxacin
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ofloxacin

Product NDC: 55111-162
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077098
Marketing Category: ANDA
Start Marketing Date: 20060210

Package Information of Ofloxacin

Package NDC: 55111-162-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-162-78) > 10 TABLET, COATED in 1 BLISTER PACK

NDC Information of Ofloxacin

NDC Code 55111-162-78
Proprietary Name Ofloxacin
Package Description 10 BLISTER PACK in 1 CARTON (55111-162-78) > 10 TABLET, COATED in 1 BLISTER PACK
Product NDC 55111-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ofloxacin
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20060210
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
Substance Name OFLOXACIN
Strength Number 400
Strength Unit mg/1
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ofloxacin


General Information