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
- 70752-162_234e0cf8-e1c9-47a2-8fa3-8a4db929c866
- Product NDC
- 70752-162
- Form
- TABLET
- Composition / generic term
- PHENOBARBITAL
- Labeler
- QUAGEN PHARMACEUTICALS LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start / end (source format)
- 20200915
- Source listing expiry
- 20261231
Source-listed ingredients
- PHENOBARBITAL — 32.4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (70752-162-10) · 70752-162-10
- 1000 TABLET in 1 BOTTLE (70752-162-11) · 70752-162-11
- 500 TABLET in 1 BOTTLE (70752-162-14) · 70752-162-14
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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