| NDC Code | 51672-4001-2 |
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| Package Description | 500 CAPSULE in 1 BOTTLE (51672-4001-2) |
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| Product NDC | 51672-4001 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Nortriptyline Hydrochloride |
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| Non-Proprietary Name | Nortriptyline Hydrochloride |
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| Dosage Form | CAPSULE |
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| Usage | ORAL |
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| Start Marketing Date | 20000508 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075520 |
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| Manufacturer | Taro Pharmaceuticals U.S.A., Inc. |
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| Substance Name | NORTRIPTYLINE 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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