| NDC Code | 50742-665-16 |
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| Package Description | 473 mL in 1 BOTTLE (50742-665-16) |
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| Product NDC | 50742-665 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide |
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| Non-Proprietary Name | Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide |
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| Dosage Form | ELIXIR |
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| Usage | ORAL |
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| Start Marketing Date | 20210801 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Ingenus Pharmaceuticals, LLC |
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| Substance Name | ATROPINE SULFATE; HYOSCYAMINE SULFATE; PHENOBARBITAL; SCOPOLAMINE HYDROBROMIDE |
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| Strength | .0194; .1037; 16.2; .0065 |
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| Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
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| Pharmacy Classes | Anticholinergic [EPC], Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA] |
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| DEA Schedule | CIV |
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