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Phenobarbital

NDC 16571-668 · Rising Pharma Holdings, Inc.

Generic namePhenobarbital
Dosage formTABLET
RouteORAL
Active ingredient(s)PHENOBARBITAL
Strength97.2 mg/1
DEA scheduleCIV
Marketing categoryUNAPPROVED DRUG OTHER

Packages

16571-668-01 — 100 TABLET in 1 BOTTLE (16571-668-01)

16571-668-10 — 1000 TABLET in 1 BOTTLE (16571-668-10)

16571-668-50 — 500 TABLET in 1 BOTTLE (16571-668-50)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

13811-299 — Phenobarbital, 13811-300 — Phenobarbital, 13811-301 — Phenobarbital, 13811-302 — Phenobarbital, 13811-303 — Phenobarbital, 13811-304 — Phenobarbital, 13811-305 — Phenobarbital, 13811-306 — Phenobarbital, 13811-307 — Phenobarbital, 16571-667 — Phenobarbital, 16571-669 — Phenobarbital, 16571-670 — Phenobarbital, 16571-671 — Phenobarbital, 16571-672 — Phenobarbital, 16571-673 — Phenobarbital, 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, +151 more

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