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Prednisolone - 68788-9096-2 - (Prednisolone)

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Drug Information of Prednisolone

Product NDC: 68788-9096
Proprietary Name: Prednisolone
Non Proprietary Name: Prednisolone
Active Ingredient(s): 15    mg/5mL & nbsp;   Prednisolone
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Prednisolone

Product NDC: 68788-9096
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040401
Marketing Category: ANDA
Start Marketing Date: 20030227

Package Information of Prednisolone

Package NDC: 68788-9096-2
Package Description: 1 BOTTLE in 1 CARTON (68788-9096-2) > 240 mL in 1 BOTTLE

NDC Information of Prednisolone

NDC Code 68788-9096-2
Proprietary Name Prednisolone
Package Description 1 BOTTLE in 1 CARTON (68788-9096-2) > 240 mL in 1 BOTTLE
Product NDC 68788-9096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prednisolone
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20030227
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name PREDNISOLONE
Strength Number 15
Strength Unit mg/5mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Prednisolone


General Information