| NDC Code | 47335-306-83 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-83) |
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| Product NDC | 47335-306 |
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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 | 20180522 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202917 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | METFORMIN HYDROCHLORIDE |
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| Strength | 1000 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Biguanide [EPC], Biguanides [CS] |
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