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Prednisolone Acetate - 54868-4293-2 - (Prednisolone Acetate)

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Drug Information of Prednisolone Acetate

Product NDC: 54868-4293
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
Coding System: National Drug Codes(NDC)

Labeler Information of Prednisolone Acetate

Product NDC: 54868-4293
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017469
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20021104

Package Information of Prednisolone Acetate

Package NDC: 54868-4293-2
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (54868-4293-2) > 5 mL in 1 BOTTLE, PLASTIC

NDC Information of Prednisolone Acetate

NDC Code 54868-4293-2
Proprietary Name Prednisolone Acetate
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (54868-4293-2) > 5 mL in 1 BOTTLE, PLASTIC
Product NDC 54868-4293
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisolone Acetate
Dosage Form Name SUSPENSION
Route Name OPHTHALMIC
Start Marketing Date 20021104
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Physicians Total Care, 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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