| NDC Code | 60687-265-32 |
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| Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-265-32) / 1 CAPSULE in 1 BLISTER PACK (60687-265-33) |
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| Product NDC | 60687-265 |
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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 | 20170124 |
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| End Marketing Date | 20231031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075520 |
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| Manufacturer | American Health Packaging |
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| Substance Name | NORTRIPTYLINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
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