Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide

NDC 50742-665 · Ingenus Pharmaceuticals, LLC

Generic namePhenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide

Dosage formELIXIR

RouteORAL

Active ingredient(s)PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE

Strength.0194; .1037; 16.2; .0065 mg/5mL; mg/5mL; mg/5mL; mg/5mL

Pharmacologic classAnticholinergic [EPC], Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

50742-665-04 — 118 mL in 1 BOTTLE (50742-665-04)

50742-665-16 — 473 mL in 1 BOTTLE (50742-665-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43353-083 — DIPHENOXYLATE HYDROCHLORIDE and ATROPINE SULFATE, 43353-594 — Diphenoxylate Hydrochloride and Atropine Sulfate, 43857-0619 — Carduus Marianus, Gentiana Lutea, Sambucus Nigra, Senna (Cassia Angustifolia), Stomach (Bovine), Arsenicum Album, Atropinum Sulphuricum,…, 43857-0644 — Carduus Marianus, Gentiana Lutea, Sambucus Nigra, Senna (Cassia Angustifolia), Stomach (Suis), Arsenicum Album, Atropinum Sulphuricum,…, 50090-3456 — Diphenoxylate Hydrochloride and Atropine Sulfate, 50090-5589 — diphenoxylate hydrochloride and atropine sulfate, 50090-5592 — diphenoxylate hydrochloride and atropine sulfate, 50090-5924 — Atropine Sulfate, 50090-7000 — Atropine Sulfate, 50090-7313 — atropine sulfate, 50742-666 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide, 50742-667 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide, 51293-694 — phenobarbital, 51525-0115 — hyoscyamine sulfate, 51655-764 — Hyoscyamine Sulfate, 51655-845 — hyoscyamine sulfate, 51662-1207 — ATROPINE SULFATE, 51662-1208 — ATROPINE SULFATE, 51662-1289 — ATROPINE SULFATE, 51662-1311 — ATROPINE SULFATE, +327 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.