Phenobarbital

NDC 70518-4129 · REMEDYREPACK INC.

Generic namePhenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength32.4 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

70518-4129-0 — 30 TABLET in 1 BLISTER PACK (70518-4129-0)

70518-4129-1 — 30 TABLET in 1 BLISTER PACK (70518-4129-1)

FDA lists these products with the same active ingredient.

69367-444 — Phenobarbital, 69367-445 — Phenobarbital, 69367-625 — Phenobarbital, 69367-626 — Phenobarbital, 69367-627 — Phenobarbital, 69367-628 — Phenobarbital, 69367-691 — Phenobarbital, 69367-692 — Phenobarbital, 69367-693 — Phenobarbital, 69367-694 — Phenobarbital, 70518-4215 — Phenobarbital, 70518-4717 — Phenobarbital, 70518-4718 — Phenobarbital, 70518-4719 — Phenobarbital, 70518-4720 — Phenobarbital, 70752-161 — PHENOBARBITAL, 70752-162 — PHENOBARBITAL, 70752-163 — PHENOBARBITAL, 70752-164 — PHENOBARBITAL, 70752-165 — 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.