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Methylprednisolone Acetate - 0703-0031-04 - (Methylprednisolone Acetate)

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Drug Information of Methylprednisolone Acetate

Product NDC: 0703-0031
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: 0703-0031
Labeler Name: Teva Parenteral Medicines, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040557
Marketing Category: ANDA
Start Marketing Date: 20050308

Package Information of Methylprednisolone Acetate

Package NDC: 0703-0031-04
Package Description: 25 VIAL, GLASS in 1 CARTON (0703-0031-04) > 1 mL in 1 VIAL, GLASS

NDC Information of Methylprednisolone Acetate

NDC Code 0703-0031-04
Proprietary Name Methylprednisolone Acetate
Package Description 25 VIAL, GLASS in 1 CARTON (0703-0031-04) > 1 mL in 1 VIAL, GLASS
Product NDC 0703-0031
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 20050308
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, 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


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