| NDC Code | 68180-199-06 |
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| Package Description | 30 TABLET in 1 BOTTLE (68180-199-06) |
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| Product NDC | 68180-199 |
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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 | 20140108 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201586 |
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| Manufacturer | Lupin Pharmaceuticals, Inc. |
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| Substance Name | AMLODIPINE BESYLATE; TELMISARTAN |
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| Strength | 10; 80 |
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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], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
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