Phenobarbital

NDC 58118-1626 · Clinical Solutions Wholesale, LLC

Generic namephenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength32.4 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

58118-1626-8 — 30 TABLET in 1 BLISTER PACK (58118-1626-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

51672-5331 — Phenobarbital, 51672-5332 — Phenobarbital, 51672-5333 — Phenobarbital, 51672-5334 — Phenobarbital, 54288-163 — Phenobarbital Oral, 58118-0572 — PHENOBARBITAL, 58118-0573 — PHENOBARBITAL, 58118-0574 — PHENOBARBITAL, 58118-0576 — PHENOBARBITAL, 58118-0626 — phenobarbital, 59212-422 — phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide, 59212-423 — phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide, 59212-425 — PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE, 60687-671 — phenobarbital, 62135-405 — phenobarbital, 62135-406 — phenobarbital, 62135-407 — phenobarbital, 62135-408 — phenobarbital, 62135-409 — phenobarbital, 62135-410 — 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.