| NDC Code | 59762-0407-4 |
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| Package Description | 1 BLISTER PACK in 1 CARTON (59762-0407-4) / 4 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
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| Product NDC | 59762-0407 |
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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, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20180302 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA022560 |
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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 | 30.1; 4.9 |
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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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