United States · FDA National Drug Code directory
Baclofen
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
- 72162-1080_3bef8995-272b-4e6e-ac32-5d61a3708b22
- Product NDC
- 72162-1080
- Form
- TABLET
- Composition / generic term
- baclofen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20051220
- Source listing expiry
- 20261231
Source-listed ingredients
- BACLOFEN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 TABLET in 1 BOTTLE, PLASTIC (72162-1080-0) · 72162-1080-0
- 100 TABLET in 1 BOTTLE, PLASTIC (72162-1080-1) · 72162-1080-1
- 30 TABLET in 1 BOTTLE, PLASTIC (72162-1080-3) · 72162-1080-3
- 500 TABLET in 1 BOTTLE, PLASTIC (72162-1080-5) · 72162-1080-5
- 60 TABLET in 1 BOTTLE, PLASTIC (72162-1080-6) · 72162-1080-6
- 90 TABLET in 1 BOTTLE, PLASTIC (72162-1080-9) · 72162-1080-9
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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