| NDC Code | 53002-4911-0 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (53002-4911-0) |
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| Product NDC | 53002-4911 |
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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 | 20210526 |
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| End Marketing Date | 20241231 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA214548 |
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| Manufacturer | RPK Pharmaceuticals, Inc. |
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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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