| NDC Code | 59762-0406-1 |
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| Package Description | 1 TABLET, FILM COATED in 1 DOSE PACK (59762-0406-1) |
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| Product NDC | 59762-0406 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Risedronate Sodium |
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| Non-Proprietary Name | Risedronate Sodium |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20080422 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA020835 |
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| Manufacturer | Mylan Pharmaceuticals, Inc. |
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| Substance Name | RISEDRONATE SODIUM HEMIPENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE |
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| Strength | 129; 21 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Bisphosphonate [EPC], Bisphosphonate [EPC], Diphosphonates [CS], Diphosphonates [CS] |
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