| NDC Code | 35573-107-49 |
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| Package Description | 1 TUBE in 1 CARTON (35573-107-49) / 50 g in 1 TUBE |
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| Product NDC | 35573-107 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Betamethasone Dipropionate |
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| Non-Proprietary Name | Betamethasone Dipropionate |
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| Dosage Form | OINTMENT, AUGMENTED |
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| Usage | TOPICAL |
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| Start Marketing Date | 20250115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA218289 |
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| Manufacturer | Burel Pharmaceuticals, LLC |
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| Substance Name | BETAMETHASONE DIPROPIONATE |
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| Strength | .5 |
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| Strength Unit | mg/g |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC] |
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