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
- 16571-675_a84eee2c-e36f-478c-8793-b153799ea38b
- Product NDC
- 16571-675
- Form
- LIQUID
- Composition / generic term
- Phenobarbital
- Labeler
- Rising Pharma Holdings, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20200901
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENOBARBITAL — 20 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 473 mL in 1 BOTTLE (16571-675-16) · 16571-675-16
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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