| NDC Code | 71914-162-16 |
|---|
| Package Description | 473 mL in 1 BOTTLE (71914-162-16) |
|---|
| Product NDC | 71914-162 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Phenobarbital With Belladonna Alkaloids |
|---|
| Non-Proprietary Name | Phenobarbital With Belladonna Alkaloids |
|---|
| Dosage Form | ELIXIR |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20180420 |
|---|
| End Marketing Date | 20210729 |
|---|
| Marketing Category Name | UNAPPROVED DRUG OTHER |
|---|
| Manufacturer | Lazarus Pharmaceuticals, Inc. |
|---|
| Substance Name | PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE |
|---|
| Strength | 16.2; .1037; .0194; .0065 |
|---|
| Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
|---|
| Pharmacy Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA] |
|---|
| DEA Schedule | CIV |
|---|