| NDC Code | 70710-1229-0 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (70710-1229-0) |
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| Product NDC | 70710-1229 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amitriptyline Hydrochloride |
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| Non-Proprietary Name | Amitriptyline Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20171226 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA210086 |
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| Manufacturer | Zydus Pharmaceuticals USA Inc. |
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| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
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| Strength | 100 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
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