| NDC Code | 40042-048-05 |
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| Package Description | 5 mL in 1 VIAL, MULTI-DOSE (40042-048-05) |
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| Product NDC | 40042-048 |
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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 | 20090731 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090747 |
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| Manufacturer | PharmaForce, 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 [EPC],Corticosteroid Hormone Receptor Agonists [MoA],Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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