| NDC Code | 51672-1390-4 |
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| Package Description | 1 BOTTLE in 1 CARTON (51672-1390-4) / 60 g in 1 BOTTLE |
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| Product NDC | 51672-1390 |
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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 | SPRAY |
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| Usage | TOPICAL |
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| Start Marketing Date | 20200617 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211722 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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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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