| NDC Code | 68180-197-07 |
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| Package Description | 90 TABLET in 1 BOTTLE (68180-197-07) |
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| Product NDC | 68180-197 |
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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 | TELMISARTAN; AMLODIPINE BESYLATE |
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| Strength | 40; 10 |
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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 [Chemical/Ingredient] |
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