NDC Code | 17856-0423-9 |
Package Description | 10 mL in 1 CUP (17856-0423-9) |
Product NDC | 17856-0423 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Donnatal |
Non-Proprietary Name | Phenobarbital |
Dosage Form | ELIXIR |
Usage | ORAL |
Start Marketing Date | 20091101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Manufacturer | Atlantic Biologicals Corps |
Substance Name | PHENOBARBITAL; HYOSCYAMINE SULFATE; SCOPOLAMINE HYDROBROMIDE; ATROPINE SULFATE |
Strength | 16.2; .1037; .0065; .0194 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL; mg/5mL |
Pharmacy Classes | Anticholinergic [EPC],Cholinergic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |
DEA Schedule | CIV |