Phenobarbital

NDC 69367-212 · Westminster Pharmaceuticals, LLC

Generic namePhenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength32.4 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

69367-212-01 — 100 TABLET in 1 BOTTLE, PLASTIC (69367-212-01)

69367-212-10 — 1000 TABLET in 1 BOTTLE, PLASTIC (69367-212-10)

FDA lists these products with the same active ingredient.

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, 68999-962 — Phenobarbital, 69367-211 — Phenobarbital, 69367-213 — Phenobarbital, 69367-214 — Phenobarbital, 69367-357 — Phenobarbital, 69367-367 — Phenobarbital, 69367-438 — Phenobarbital, 69367-439 — Phenobarbital, 69367-440 — Phenobarbital, 69367-441 — Phenobarbital, 69367-442 — Phenobarbital, 69367-443 — 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.