| NDC Code | 69367-199-01 |
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| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (69367-199-01) |
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| Product NDC | 69367-199 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Doxylamine Succinate And Phenylephrine Hydrochloride |
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| Non-Proprietary Name | Doxylamine Succinate And Phenylephrine Hydrochloride |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20181025 |
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| End Marketing Date | 20240501 |
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| Marketing Category Name | OTC MONOGRAPH FINAL |
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| Application Number | part341 |
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| Manufacturer | Westminster Pharmaceuticals, LLC |
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| Substance Name | DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE |
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| Strength | 7.5; 10 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Adrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC] |
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