| NDC Code | 0555-0779-04 |
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| Package Description | 500 TABLET in 1 BOTTLE (0555-0779-04) |
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| Product NDC | 0555-0779 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Medroxyprogesterone Acetate |
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| Non-Proprietary Name | Medroxyprogesterone Acetate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19961204 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040159 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | MEDROXYPROGESTERONE ACETATE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Progesterone Congeners [CS], Progestin [EPC] |
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