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
- 64950-578_ec88f9c0-b075-49a7-acda-8dc7a84b2aee
- Product NDC
- 64950-578
- Form
- TABLET
- Composition / generic term
- PHENOBARBITAL
- Labeler
- Genus Lifesciences
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20250301
- Source listing expiry
- 20271231
Source-listed ingredients
- PHENOBARBITAL — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (64950-578-01) · 64950-578-01
- 1000 TABLET in 1 BOTTLE (64950-578-10) · 64950-578-10
Source and coverage
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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.
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