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Methylprednisolone - 0703-0063-01 - (Methylprednisolone acetate)

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Drug Information of Methylprednisolone

Product NDC: 0703-0063
Proprietary Name: Methylprednisolone
Non Proprietary Name: Methylprednisolone acetate
Active Ingredient(s): 80    mg/mL & nbsp;   Methylprednisolone acetate
Administration Route(s): INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Methylprednisolone

Product NDC: 0703-0063
Labeler Name: Teva Parenteral Medicines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040620
Marketing Category: ANDA
Start Marketing Date: 20061031

Package Information of Methylprednisolone

Package NDC: 0703-0063-01
Package Description: 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0063-01) > 5 mL in 1 VIAL, MULTI-DOSE

NDC Information of Methylprednisolone

NDC Code 0703-0063-01
Proprietary Name Methylprednisolone
Package Description 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0063-01) > 5 mL in 1 VIAL, MULTI-DOSE
Product NDC 0703-0063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylprednisolone acetate
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE
Start Marketing Date 20061031
Marketing Category Name ANDA
Labeler Name Teva Parenteral Medicines, Inc
Substance Name METHYLPREDNISOLONE ACETATE
Strength Number 80
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone


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