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
- 71335-2767_5bae76d2-2bf4-4353-ac07-0156403a7cf1
- Product NDC
- 71335-2767
- Form
- TABLET
- Composition / generic term
- Baclofen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240615
- Source listing expiry
- 20261231
Source-listed ingredients
- BACLOFEN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 112 TABLET in 1 BLISTER PACK (71335-2767-0) · 71335-2767-0
- 30 TABLET in 1 BLISTER PACK (71335-2767-1) · 71335-2767-1
- 120 TABLET in 1 BLISTER PACK (71335-2767-2) · 71335-2767-2
- 20 TABLET in 1 BLISTER PACK (71335-2767-3) · 71335-2767-3
- 60 TABLET in 1 BLISTER PACK (71335-2767-4) · 71335-2767-4
- 100 TABLET in 1 BLISTER PACK (71335-2767-5) · 71335-2767-5
- 56 TABLET in 1 BLISTER PACK (71335-2767-6) · 71335-2767-6
- 90 TABLET in 1 BLISTER PACK (71335-2767-7) · 71335-2767-7
- 140 TABLET in 1 BLISTER PACK (71335-2767-8) · 71335-2767-8
- 84 TABLET in 1 BLISTER PACK (71335-2767-9) · 71335-2767-9
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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