| NDC Code | 0046-1105-51 |
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| Package Description | 1 POUCH in 1 CARTON (0046-1105-51) > 1 BLISTER PACK in 1 POUCH > 5 TABLET, SUGAR COATED in 1 BLISTER PACK |
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| Product NDC | 0046-1105 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Prempro |
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| Non-Proprietary Name | Conjugated Estrogens And Medroxyprogesterone Acetate |
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| Dosage Form | TABLET, SUGAR COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20090921 |
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| Marketing Category Name | NDA |
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| Application Number | NDA020527 |
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| Manufacturer | Wyeth Pharmaceuticals Inc., a subsidiary of Pfizer Inc. |
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| Substance Name | ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE |
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| Strength | .3; 1.5 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Estrogen [EPC],Estrogen Receptor Agonists [MoA],Estrogens, Conjugated (USP) [Chemical/Ingredient],Progesterone Congeners [Chemical/Ingredient],Progestin [EPC] |
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