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Depo-Medrol
Depo-Medrol - 0009-0280-03 - (methylprednisolone acetate)
Drug Information of Depo-Medrol
| Product NDC: | 0009-0280 |
| Proprietary Name: | Depo-Medrol |
| Non Proprietary Name: | methylprednisolone acetate |
| Active Ingredient(s): | 40 mg/mL & nbsp; methylprednisolone acetate |
| Administration Route(s): | INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
| Dosage Form(s): | INJECTION, SUSPENSION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Depo-Medrol
| Product NDC: | 0009-0280 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011757 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19590528 |
Package Information of Depo-Medrol
| Package NDC: | 0009-0280-03 |
| Package Description: | 10 mL in 1 VIAL, MULTI-DOSE (0009-0280-03) |
NDC Information of Depo-Medrol
| NDC Code | 0009-0280-03 |
| Proprietary Name | Depo-Medrol |
| Package Description | 10 mL in 1 VIAL, MULTI-DOSE (0009-0280-03) |
| Product NDC | 0009-0280 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | methylprednisolone acetate |
| Dosage Form Name | INJECTION, SUSPENSION |
| Route Name | INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
| Start Marketing Date | 19590528 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | METHYLPREDNISOLONE ACETATE |
| Strength Number | 40 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
