NDC Code | 17856-0162-1 |
Package Description | 10 mL in 1 CUP, UNIT-DOSE (17856-0162-1) |
Product NDC | 17856-0162 |
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 | 20180521 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Manufacturer | ATLANTIC BIOLOGICALS CORP. |
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] |