United States · FDA National Drug Code directory
Phenobarbital
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 72162-1265_0308bc99-4ace-43f0-9d40-cfef627ad1a8
- Product NDC
- 72162-1265
- Form
- TABLET
- Composition / generic term
- Phenobarbital
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20201101
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENOBARBITAL — 64.8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (72162-1265-0) · 72162-1265-0
- 100 TABLET in 1 BOTTLE (72162-1265-1) · 72162-1265-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →