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
- 71205-848_6cf88fef-0c82-4d5d-85e8-5896ac013165
- Product NDC
- 71205-848
- Form
- TABLET
- Composition / generic term
- Phenobarbital
- Labeler
- Proficient Rx LP
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20201101
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENOBARBITAL — 60 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (71205-848-00) · 71205-848-00
- 1000 TABLET in 1 BOTTLE (71205-848-11) · 71205-848-11
- 30 TABLET in 1 BOTTLE (71205-848-30) · 71205-848-30
- 500 TABLET in 1 BOTTLE (71205-848-55) · 71205-848-55
- 60 TABLET in 1 BOTTLE (71205-848-60) · 71205-848-60
- 240 TABLET in 1 BOTTLE (71205-848-64) · 71205-848-64
- 120 TABLET in 1 BOTTLE (71205-848-72) · 71205-848-72
- 180 TABLET in 1 BOTTLE (71205-848-78) · 71205-848-78
- 90 TABLET in 1 BOTTLE (71205-848-90) · 71205-848-90
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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