ofloxacin - 16571-130-11 - (ofloxacin)

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Drug Information of ofloxacin

Product NDC: 16571-130
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: 16571-130
Labeler Name: Pack Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078559
Marketing Category: ANDA
Start Marketing Date: 20100104

Package Information of ofloxacin

Package NDC: 16571-130-11
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (16571-130-11) > 10 mL in 1 BOTTLE, PLASTIC

NDC Information of ofloxacin

NDC Code 16571-130-11
Proprietary Name ofloxacin
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (16571-130-11) > 10 mL in 1 BOTTLE, PLASTIC
Product NDC 16571-130
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ofloxacin
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20100104
Marketing Category Name ANDA
Labeler Name Pack Pharmaceuticals, LLC
Substance Name OFLOXACIN
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Quinolone Antimicrobial [EPC],Quinolones [Chemical/Ingredient]

Complete Information of ofloxacin


General Information