Phenobarbital

NDC 62135-412 · Chartwell RX, LLC

Generic namephenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength100 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

62135-412-05 — 500 TABLET in 1 BOTTLE (62135-412-05)

62135-412-90 — 90 TABLET in 1 BOTTLE (62135-412-90)

FDA lists these products with the same active ingredient.

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, 62135-411 — phenobarbital, 62135-962 — Phenobarbital, 63187-895 — phenobarbital, 63629-2289 — phenobarbital, 63629-2399 — Phenobarbital, 63629-2400 — Phenobarbital, 63629-2401 — Phenobarbital, 63629-2402 — Phenobarbital, 63629-2403 — Phenobarbital, 63629-2404 — Phenobarbital, 64380-166 — 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.