| NDC Code | 50419-483-72 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (50419-483-72) / 14 TABLET, FILM COATED in 1 BLISTER PACK (50419-483-71) |
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| Product NDC | 50419-483 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Angeliq |
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| Non-Proprietary Name | Drospirenone And Estradiol |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20051128 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021355 |
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| Manufacturer | Bayer HealthCare Pharmaceuticals Inc. |
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| Substance Name | DROSPIRENONE; ESTRADIOL |
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| Strength | .5; 1 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Estradiol Congeners [CS], Estrogen Receptor Agonists [MoA], Estrogen [EPC], Progesterone Congeners [CS], Progestin [EPC] |
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