| NDC Code | 0517-0791-01 |
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| Package Description | 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0791-01) / 5 mL in 1 VIAL, MULTI-DOSE |
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| Product NDC | 0517-0791 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Betamethasone Sodium Phosphate And Betamethasone Acetate |
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| Non-Proprietary Name | Betamethasone Sodium Phosphate And Betamethasone Acetate |
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| Dosage Form | INJECTION, SUSPENSION |
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| Usage | INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR |
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| Start Marketing Date | 20191101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090747 |
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| Manufacturer | American Regent, Inc. |
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| Substance Name | BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE |
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| Strength | 3; 3 |
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| Strength Unit | mg/mL; mg/mL |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Corticosteroid [EPC] |
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