Phenobarbital

NDC 51672-5329 · Sun Pharmaceutical Industries, Inc.

Generic namePhenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength97.2 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

51672-5329-1 — 100 TABLET in 1 BOTTLE, PLASTIC (51672-5329-1)

51672-5329-3 — 1000 TABLET in 1 BOTTLE, PLASTIC (51672-5329-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16571-674 — Phenobarbital, 16571-675 — Phenobarbital, 17856-0125 — Phenobarbital, Hyoscyamine Sulfate, Atropine sulfate, and Scopolamine Hydrobromide, 50742-665 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide, 50742-666 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide, 50742-667 — Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide, 51293-694 — phenobarbital, 51672-5326 — Phenobarbital, 51672-5327 — Phenobarbital, 51672-5328 — Phenobarbital, 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, +151 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.