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
- 70756-289_97901dd3-f1e0-4fc8-86a1-5114e2095073
- Product NDC
- 70756-289
- Form
- TABLET
- Composition / generic term
- Baclofen
- Labeler
- Lifestar Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220126
- 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 (70756-289-11) · 70756-289-11
- 1000 TABLET in 1 BOTTLE (70756-289-12) · 70756-289-12
- 500 TABLET in 1 BOTTLE (70756-289-51) · 70756-289-51
- 10 BLISTER PACK in 1 CARTON (70756-289-99) / 10 TABLET in 1 BLISTER PACK (70756-289-01) · 70756-289-99
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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