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
- 72789-480_4de00cd5-cc95-40b3-e063-6394a90a448c
- Product NDC
- 72789-480
- Form
- TABLET
- Composition / generic term
- BACLOFEN
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180401
- Source listing expiry
- 20271231
Source-listed ingredients
- BACLOFEN — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (72789-480-01) · 72789-480-01
- 90 TABLET in 1 BOTTLE, PLASTIC (72789-480-90) · 72789-480-90
- 1000 TABLET in 1 BOTTLE, PLASTIC (72789-480-95) · 72789-480-95
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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