| NDC Code | 69452-206-20 |
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| Package Description | 100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-206-20) |
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| Product NDC | 69452-206 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Doxylamine Succinate And Pyridoxine Hydrochloride |
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| Non-Proprietary Name | Doxylamine Succinate And Pyridoxine Hydrochloride |
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| Dosage Form | TABLET, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20231211 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA217000 |
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| Manufacturer | Bionpharma Inc., |
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| Substance Name | DOXYLAMINE SUCCINATE; PYRIDOXINE HYDROCHLORIDE |
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| Strength | 10; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Analogs/Derivatives [Chemical/Ingredient], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], Vitamin B 6 [Chemical/Ingredient], Vitamin B6 Analog [EPC] |
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