| NDC Code | 21922-104-01 |
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| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (21922-104-01) / 60 mL in 1 BOTTLE, PLASTIC |
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| Product NDC | 21922-104 |
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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 | LOTION, AUGMENTED |
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| Usage | TOPICAL |
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| Start Marketing Date | 20251125 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA206389 |
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| Manufacturer | Encube Ethicals, Inc. |
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| Substance Name | BETAMETHASONE DIPROPIONATE |
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| Strength | .5 |
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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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