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Phenobarbital

NDC 69367-439 · Westminster Pharmaceuticals, LLC

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

Packages

69367-439-01 — 100 TABLET in 1 BOTTLE (69367-439-01)

69367-439-10 — 1000 TABLET in 1 BOTTLE (69367-439-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 69367-438 — 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, 69367-628 — 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.