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Methylprednisolone Acetate - 21695-850-05 - (Methylprednisolone Acetate)

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Drug Information of Methylprednisolone Acetate

Product NDC: 21695-850
Proprietary Name: Methylprednisolone Acetate
Non Proprietary Name: Methylprednisolone Acetate
Active Ingredient(s): 80    mg/mL & nbsp;   Methylprednisolone Acetate
Administration Route(s): INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; PARENTERAL; SOFT TISSUE
Dosage Form(s): INJECTION, SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Methylprednisolone Acetate

Product NDC: 21695-850
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040794
Marketing Category: ANDA
Start Marketing Date: 20090305

Package Information of Methylprednisolone Acetate

Package NDC: 21695-850-05
Package Description: 5 mL in 1 BOTTLE (21695-850-05)

NDC Information of Methylprednisolone Acetate

NDC Code 21695-850-05
Proprietary Name Methylprednisolone Acetate
Package Description 5 mL in 1 BOTTLE (21695-850-05)
Product NDC 21695-850
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methylprednisolone Acetate
Dosage Form Name INJECTION, SUSPENSION
Route Name INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; PARENTERAL; SOFT TISSUE
Start Marketing Date 20090305
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name METHYLPREDNISOLONE ACETATE
Strength Number 80
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Methylprednisolone Acetate


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