Phenobarbital

NDC 67046-0059 · Coupler LLC

Generic namePhenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength32.4 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

67046-0059-3 — 30 TABLET in 1 BLISTER PACK (67046-0059-3)

FDA lists these products with the same active ingredient.

64380-166 — phenobarbital, 64950-571 — PHENOBARBITAL, 64950-572 — PHENOBARBITAL, 64950-573 — PHENOBARBITAL, 64950-574 — PHENOBARBITAL, 64950-575 — PHENOBARBITAL, 64950-576 — PHENOBARBITAL, 64950-577 — PHENOBARBITAL, 64950-578 — PHENOBARBITAL, 66689-063 — phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide, 67046-0780 — Phenobarbital, 67046-1434 — Phenobarbital, 67046-1543 — Phenobarbital, 67296-2145 — Phenobarbital, 68999-962 — Phenobarbital, 69367-211 — Phenobarbital, 69367-212 — Phenobarbital, 69367-213 — Phenobarbital, 69367-214 — Phenobarbital, 69367-357 — 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.