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Phenobarbital

NDC 75826-137 · WINDER LABORATORIES, LLC

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

Packages

75826-137-00 — 1000 TABLET in 1 BOTTLE, PLASTIC (75826-137-00)

75826-137-10 — 100 TABLET in 1 BOTTLE, PLASTIC (75826-137-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72162-1167 — phenobarbital, 72162-1168 — phenobarbital, 72162-1265 — Phenobarbital, 72162-1266 — Phenobarbital, 72162-1267 — Phenobarbital, 72162-1268 — Phenobarbital, 75826-118 — PHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDE, 75826-127 — Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide, 75826-128 — Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide, 75826-136 — Phenobarbital, 75826-138 — Phenobarbital, 75826-139 — Phenobarbital, 75826-140 — Phenobarbital, 75826-141 — Phenobarbital, 75826-142 — Phenobarbital, 75826-143 — Phenobarbital, 81033-163 — Phenobarbital Oral, 81033-164 — Phenobarbital Oral, 82804-982 — Phenobarbital, 82804-983 — 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.