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PREDNISOLONE ACETATE - 60758-119-15 - (prednisolone acetate)

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Drug Information of PREDNISOLONE ACETATE

Product NDC: 60758-119
Proprietary Name: PREDNISOLONE ACETATE
Non Proprietary Name: prednisolone acetate
Active Ingredient(s): 10    mg/mL & nbsp;   prednisolone acetate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of PREDNISOLONE ACETATE

Product NDC: 60758-119
Labeler Name: Pacific Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017011
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19970819

Package Information of PREDNISOLONE ACETATE

Package NDC: 60758-119-15
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (60758-119-15) > 15 mL in 1 BOTTLE, DROPPER

NDC Information of PREDNISOLONE ACETATE

NDC Code 60758-119-15
Proprietary Name PREDNISOLONE ACETATE
Package Description 1 BOTTLE, DROPPER in 1 CARTON (60758-119-15) > 15 mL in 1 BOTTLE, DROPPER
Product NDC 60758-119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name prednisolone acetate
Dosage Form Name SUSPENSION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19970819
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Pacific Pharma, Inc.
Substance Name PREDNISOLONE ACETATE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of PREDNISOLONE ACETATE


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