Ofloxacin - 40042-049-05 - (Ofloxacin)

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Drug Information of Ofloxacin

Product NDC: 40042-049
Proprietary Name: Ofloxacin
Non Proprietary Name: Ofloxacin
Active Ingredient(s): 3    mg/mL & nbsp;   Ofloxacin
Administration Route(s): AURICULAR (OTIC)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ofloxacin

Product NDC: 40042-049
Labeler Name: PharmaForce, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090395
Marketing Category: ANDA
Start Marketing Date: 20100121

Package Information of Ofloxacin

Package NDC: 40042-049-05
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (40042-049-05) > 5 mL in 1 BOTTLE, PLASTIC

NDC Information of Ofloxacin

NDC Code 40042-049-05
Proprietary Name Ofloxacin
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (40042-049-05) > 5 mL in 1 BOTTLE, PLASTIC
Product NDC 40042-049
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ofloxacin
Dosage Form Name SOLUTION
Route Name AURICULAR (OTIC)
Start Marketing Date 20100121
Marketing Category Name ANDA
Labeler Name PharmaForce, 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