| NDC Code | 58118-2212-0 |
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| Package Description | 1 TABLET, FILM COATED in 1 PACKET (58118-2212-0) |
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| Product NDC | 58118-2212 |
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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 | 19970911 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA040218 |
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| Manufacturer | Clinical Solutions Wholesale |
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| Substance Name | AMITRIPTYLINE HYDROCHLORIDE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
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