| NDC Code | 0703-0045-01 |
|---|
| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0703-0045-01) / 10 mL in 1 VIAL, MULTI-DOSE |
|---|
| Product NDC | 0703-0045 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Methylprednisolone Acetate |
|---|
| Non-Proprietary Name | Methylprednisolone Acetate |
|---|
| Dosage Form | INJECTION, SUSPENSION |
|---|
| Usage | INTRALESIONAL; INTRAMUSCULAR; INTRASYNOVIAL; SOFT TISSUE |
|---|
| Start Marketing Date | 20061031 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040620 |
|---|
| Manufacturer | Teva Parenteral Medicines, Inc. |
|---|
| Substance Name | METHYLPREDNISOLONE ACETATE |
|---|
| Strength | 40 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
|---|