Phenobarbital

NDC 69367-438 · Westminster Pharmaceuticals, LLC

Generic namePhenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength15 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

69367-438-01 — 100 TABLET in 1 BOTTLE (69367-438-01)

69367-438-05 — 500 TABLET in 1 BOTTLE (69367-438-05)

FDA lists these products with the same active ingredient.

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, 69367-367 — Phenobarbital, 69367-439 — Phenobarbital, 69367-440 — Phenobarbital, 69367-441 — Phenobarbital, 69367-442 — Phenobarbital, 69367-443 — Phenobarbital, 69367-444 — Phenobarbital, 69367-445 — Phenobarbital, 69367-625 — Phenobarbital, 69367-626 — Phenobarbital, 69367-627 — 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.