| NDC Code | 69367-389-10 |
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| Package Description | 1000 TABLET, COATED in 1 BOTTLE (69367-389-10) |
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| Product NDC | 69367-389 |
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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, COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20240520 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212654 |
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| Manufacturer | Westminster Pharmaceuticals, LLC |
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| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
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| Strength | 25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
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