| NDC Code | 0703-0051-01 |
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| Package Description | 1 VIAL, SINGLE-DOSE in 1 CARTON (0703-0051-01) / 1 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 0703-0051 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Methylprednisolone Acetate |
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| Non-Proprietary Name | Methylprednisolone Acetate |
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| Dosage Form | INJECTION, SUSPENSION |
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| Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; SOFT TISSUE |
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| Start Marketing Date | 20050308 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040557 |
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| Manufacturer | Teva Parenteral Medicines, Inc. |
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| Substance Name | METHYLPREDNISOLONE ACETATE |
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| Strength | 80 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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