Ofloxacin - 52125-656-01 - (Ofloxacin)

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Drug Information of Ofloxacin

Product NDC: 52125-656
Proprietary Name: Ofloxacin
Non Proprietary Name: Ofloxacin
Active Ingredient(s): 3    mg/mL & nbsp;   Ofloxacin
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ofloxacin

Product NDC: 52125-656
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076231
Marketing Category: ANDA
Start Marketing Date: 20130701

Package Information of Ofloxacin

Package NDC: 52125-656-01
Package Description: 5 mL in 1 BOTTLE (52125-656-01)

NDC Information of Ofloxacin

NDC Code 52125-656-01
Proprietary Name Ofloxacin
Package Description 5 mL in 1 BOTTLE (52125-656-01)
Product NDC 52125-656
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ofloxacin
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20130701
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name OFLOXACIN
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of Ofloxacin


General Information