| NDC Code | 46708-185-08 |
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| Package Description | 80 BLISTER PACK in 1 CARTON (46708-185-08) / 8 TABLET in 1 BLISTER PACK |
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| Product NDC | 46708-185 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Telmisartan And Amlodipine |
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| Non-Proprietary Name | Telmisartan And Amlodipine |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20161122 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205234 |
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| Manufacturer | Alembic Pharmaceuticals Limited |
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| Substance Name | AMLODIPINE BESYLATE; TELMISARTAN |
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| Strength | 10; 40 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
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