| NDC Code | 50383-959-10 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (50383-959-10) |
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| Product NDC | 50383-959 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Protriptyline Hydrochloride |
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| Non-Proprietary Name | Protriptyline Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20131028 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202220 |
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| Manufacturer | Hi-Tech Pharmacal Co., Inc. |
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| Substance Name | PROTRIPTYLINE HYDROCHLORIDE |
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| Strength | 5 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tricyclic Antidepressant [EPC] |
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