PHENOBARBITAL

NDC 70752-164 · QUAGEN PHARMACEUTICALS LLC

Generic namePHENOBARBITAL

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength97.2 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

70752-164-10 — 100 TABLET in 1 BOTTLE (70752-164-10)

70752-164-11 — 1000 TABLET in 1 BOTTLE (70752-164-11)

70752-164-14 — 500 TABLET in 1 BOTTLE (70752-164-14)

FDA lists these products with the same active ingredient.

69367-694 — Phenobarbital, 70518-4129 — 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, 70752-165 — PHENOBARBITAL, 70752-166 — PHENOBARBITAL, 70752-167 — PHENOBARBITAL, 70752-168 — PHENOBARBITAL, 71205-845 — Phenobarbital, 71205-846 — Phenobarbital, 71205-847 — Phenobarbital, 71205-848 — Phenobarbital, 71205-849 — Phenobarbital, 71205-850 — 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.