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Prednisolone Acetate - 61314-637-15 - (Prednisolone Acetate)

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Drug Information of Prednisolone Acetate

Product NDC: 61314-637
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: 61314-637
Labeler Name: Falcon Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017469
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 19941215

Package Information of Prednisolone Acetate

Package NDC: 61314-637-15
Package Description: 15 mL in 1 BOTTLE, PLASTIC (61314-637-15)

NDC Information of Prednisolone Acetate

NDC Code 61314-637-15
Proprietary Name Prednisolone Acetate
Package Description 15 mL in 1 BOTTLE, PLASTIC (61314-637-15)
Product NDC 61314-637
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisolone Acetate
Dosage Form Name SUSPENSION
Route Name OPHTHALMIC
Start Marketing Date 19941215
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Falcon Pharmaceuticals
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