| NDC Code | 71914-162-04 |
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| Package Description | 120 mL in 1 BOTTLE (71914-162-04) |
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| Product NDC | 71914-162 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Phenobarbital With Belladonna Alkaloids |
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| Non-Proprietary Name | Phenobarbital With Belladonna Alkaloids |
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| Dosage Form | ELIXIR |
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| Usage | ORAL |
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| Start Marketing Date | 20180420 |
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| End Marketing Date | 20210729 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | Lazarus Pharmaceuticals, Inc. |
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| Substance Name | PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE |
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| Strength | 16.2; .1037; .0194; .0065 |
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| Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
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| Pharmacy Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
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| DEA Schedule | CIV |
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