Phenobarbital

NDC 16571-674 · Rising Pharma Holdings, Inc.

Generic namePhenobarbital

Dosage formTABLET

RouteORAL

Active ingredient(s)PHENOBARBITAL

Strength60 mg/1

DEA scheduleCIV

Marketing categoryUNAPPROVED DRUG OTHER

Packages

16571-674-01 — 100 TABLET in 1 BOTTLE (16571-674-01)

16571-674-10 — 1000 TABLET in 1 BOTTLE (16571-674-10)

16571-674-50 — 500 TABLET in 1 BOTTLE (16571-674-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13811-305 — Phenobarbital, 13811-306 — Phenobarbital, 13811-307 — Phenobarbital, 16571-667 — Phenobarbital, 16571-668 — Phenobarbital, 16571-669 — Phenobarbital, 16571-670 — Phenobarbital, 16571-671 — Phenobarbital, 16571-672 — Phenobarbital, 16571-673 — 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, 51672-5329 — 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.