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PHENOBARBITAL

NDC 70752-161 · QUAGEN PHARMACEUTICALS LLC

Generic namePHENOBARBITAL
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENOBARBITAL
Strength16.2 mg/1
DEA scheduleCIV
Marketing categoryUNAPPROVED DRUG OTHER

Packages

70752-161-10 — 100 TABLET in 1 BOTTLE (70752-161-10)

70752-161-11 — 1000 TABLET in 1 BOTTLE (70752-161-11)

70752-161-14 — 500 TABLET in 1 BOTTLE (70752-161-14)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-691 — Phenobarbital, 69367-692 — Phenobarbital, 69367-693 — Phenobarbital, 69367-694 — Phenobarbital, 70518-4129 — Phenobarbital, 70518-4215 — Phenobarbital, 70518-4717 — Phenobarbital, 70518-4718 — Phenobarbital, 70518-4719 — Phenobarbital, 70518-4720 — Phenobarbital, 70752-162 — PHENOBARBITAL, 70752-163 — PHENOBARBITAL, 70752-164 — PHENOBARBITAL, 70752-165 — PHENOBARBITAL, 70752-166 — PHENOBARBITAL, 70752-167 — PHENOBARBITAL, 70752-168 — PHENOBARBITAL, 71205-845 — Phenobarbital, 71205-846 — Phenobarbital, 71205-847 — 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.