| NDC Code | 0781-7165-35 |
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| Package Description | 1 TUBE in 1 CARTON (0781-7165-35) / 60 g in 1 TUBE |
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| Product NDC | 0781-7165 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Calcipotriene And Betamethasone Dipropionate |
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| Non-Proprietary Name | Calcipotriene And Betamethasone Dipropionate |
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| Dosage Form | OINTMENT |
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| Usage | TOPICAL |
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| Start Marketing Date | 20140331 |
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| End Marketing Date | 20240430 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201615 |
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| Manufacturer | Sandoz Inc. |
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| Substance Name | BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE |
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| Strength | .5; 50 |
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| Strength Unit | mg/g; ug/g |
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| Pharmacy Classes | Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Vitamin D Analog [EPC], Vitamin D [CS] |
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