| NDC Code | 49638-106-30 |
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| Package Description | 1 BOTTLE in 1 CARTON (49638-106-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE |
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| Product NDC | 49638-106 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Tylo Night (acetaminophen) |
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| Non-Proprietary Name | Acetaminophen |
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| Dosage Form | TABLET, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20200706 |
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| Marketing Category Name | OTC MONOGRAPH DRUG |
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| Application Number | M013 |
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| Manufacturer | America Medic & Science, LLC |
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| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 500; 25 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC] |
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