| NDC Code | 0378-6002-91 |
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| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-6002-91) |
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| Product NDC | 0378-6002 |
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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 |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20160823 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200690 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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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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