PHENOBARBITAL

NDC 64950-574 · Genus Lifesciences

Generic namePHENOBARBITAL

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength32.4 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

64950-574-01 — 100 TABLET in 1 BOTTLE (64950-574-01)

64950-574-10 — 1000 TABLET in 1 BOTTLE (64950-574-10)

FDA lists these products with the same active ingredient.

63629-2399 — Phenobarbital, 63629-2400 — Phenobarbital, 63629-2401 — Phenobarbital, 63629-2402 — Phenobarbital, 63629-2403 — Phenobarbital, 63629-2404 — Phenobarbital, 64380-166 — phenobarbital, 64950-571 — PHENOBARBITAL, 64950-572 — PHENOBARBITAL, 64950-573 — PHENOBARBITAL, 64950-575 — PHENOBARBITAL, 64950-576 — PHENOBARBITAL, 64950-577 — PHENOBARBITAL, 64950-578 — PHENOBARBITAL, 66689-063 — phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide, 67046-0059 — Phenobarbital, 67046-0780 — Phenobarbital, 67046-1434 — Phenobarbital, 67046-1543 — Phenobarbital, 67296-2145 — 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.