| NDC Code | 73317-4256-1 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 PACKAGE (73317-4256-1) |
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| Product NDC | 73317-4256 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Metformin Hydrochloride |
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| Non-Proprietary Name | Metformin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20210416 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213334 |
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| Manufacturer | SLV PHARMACEUTICALS LLC DBA AUM PHARMACEUTICALS |
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| Substance Name | METFORMIN HYDROCHLORIDE |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Biguanide [EPC], Biguanides [CS] |
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