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PREDNISOLONE ACETATE - 52959-265-10 - (prednisolone acetate)

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Drug Information of PREDNISOLONE ACETATE

Product NDC: 52959-265
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: 52959-265
Labeler Name: H.J. Harkins Company, 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: 52959-265-10
Package Description: 10 mL in 1 BOTTLE, DROPPER (52959-265-10)

NDC Information of PREDNISOLONE ACETATE

NDC Code 52959-265-10
Proprietary Name PREDNISOLONE ACETATE
Package Description 10 mL in 1 BOTTLE, DROPPER (52959-265-10)
Product NDC 52959-265
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 H.J. Harkins Company, 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


General Information