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
- 71610-452_d28f263b-b7d3-47f4-8d3e-bc2fd5594da4
- Product NDC
- 71610-452
- Form
- TABLET
- Composition / generic term
- baclofen
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200501
- Source listing expiry
- 20261231
Source-listed ingredients
- BACLOFEN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET in 1 BOTTLE, PLASTIC (71610-452-60) · 71610-452-60
- 180 TABLET in 1 BOTTLE, PLASTIC (71610-452-80) · 71610-452-80
- 270 TABLET in 1 BOTTLE, PLASTIC (71610-452-92) · 71610-452-92
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →