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Phenobarbital

NDC 72162-1167 · Bryant Ranch Prepack

Generic namephenobarbital
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENOBARBITAL
Strength64.8 mg/1
DEA scheduleCIV
Marketing categoryUNAPPROVED DRUG OTHER

Packages

72162-1167-0 — 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1167-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-848 — Phenobarbital, 71205-849 — Phenobarbital, 71205-850 — Phenobarbital, 71205-851 — Phenobarbital, 71205-889 — Phenobarbital, 71205-890 — Phenobarbital, 71205-891 — Phenobarbital, 71205-892 — Phenobarbital, 71205-893 — Phenobarbital, 72162-1166 — phenobarbital, 72162-1168 — phenobarbital, 72162-1265 — Phenobarbital, 72162-1266 — Phenobarbital, 72162-1267 — Phenobarbital, 72162-1268 — Phenobarbital, 75826-118 — PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE, 75826-127 — Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide, 75826-128 — Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide, 75826-136 — Phenobarbital, 75826-137 — Phenobarbital, +151 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.