Home > National Drug Code (NDC) > Methylprednisolone Acetate

Methylprednisolone Acetate - 54868-0590-0 - (Methylprednisolone Acetate)

Alphabetical Index


Drug Information of Methylprednisolone Acetate

Product NDC: 54868-0590
Proprietary Name: Methylprednisolone Acetate
Non Proprietary Name: Methylprednisolone Acetate
Active Ingredient(s): 40    mg/mL & nbsp;   Methylprednisolone Acetate
Administration Route(s): INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Methylprednisolone Acetate

Product NDC: 54868-0590
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040557
Marketing Category: ANDA
Start Marketing Date: 20120726

Package Information of Methylprednisolone Acetate

Package NDC: 54868-0590-0
Package Description: 1 VIAL, GLASS in 1 CARTON (54868-0590-0) > 1 mL in 1 VIAL, GLASS

NDC Information of Methylprednisolone Acetate

NDC Code 54868-0590-0
Proprietary Name Methylprednisolone Acetate
Package Description 1 VIAL, GLASS in 1 CARTON (54868-0590-0) > 1 mL in 1 VIAL, GLASS
Product NDC 54868-0590
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylprednisolone Acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
Start Marketing Date 20120726
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name METHYLPREDNISOLONE ACETATE
Strength Number 40
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone Acetate


General Information