| NDC Code | 68180-490-03 |
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| Package Description | 1000 TABLET in 1 BOTTLE (68180-490-03) |
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| Product NDC | 68180-490 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Repaglinide And Metformin Hydrochloride |
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| Non-Proprietary Name | Repaglinide And Metformin Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20151210 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200624 |
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| Manufacturer | Lupin Pharmaceuticals, Inc. |
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| Substance Name | METFORMIN HYDROCHLORIDE; REPAGLINIDE |
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| Strength | 500; 1 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Biguanide [EPC],Biguanides [CS],Glinide [EPC],Potassium Channel Antagonists [MoA] |
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