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
- 71205-474_4702c59e-202c-4900-9388-f64788cb035c
- Product NDC
- 71205-474
- Form
- TABLET
- Composition / generic term
- Baclofen
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20110101
- Source listing expiry
- 20261231
Source-listed ingredients
- BACLOFEN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 14 TABLET in 1 BOTTLE (71205-474-14) · 71205-474-14
- 20 TABLET in 1 BOTTLE (71205-474-20) · 71205-474-20
- 30 TABLET in 1 BOTTLE (71205-474-30) · 71205-474-30
- 60 TABLET in 1 BOTTLE (71205-474-60) · 71205-474-60
- 120 TABLET in 1 BOTTLE (71205-474-72) · 71205-474-72
- 180 TABLET in 1 BOTTLE (71205-474-78) · 71205-474-78
- 90 TABLET in 1 BOTTLE (71205-474-90) · 71205-474-90
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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