| NDC Code | 68788-0972-4 |
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| Package Description | 45 g in 1 TUBE (68788-0972-4) |
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| Product NDC | 68788-0972 |
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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 |
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| Usage | TOPICAL |
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| Start Marketing Date | 19870203 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA071012 |
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| Manufacturer | Preferred Pharmaceuticals, 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 [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
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