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
- 68788-9246_b605ca0d-58f9-4995-b87e-e5b186fa9ce7
- Product NDC
- 68788-9246
- Form
- TABLET
- Composition / generic term
- baclofen
- Labeler
- Preferred Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20141022
- Source listing expiry
- 20271231
Source-listed ingredients
- BACLOFEN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (68788-9246-1) · 68788-9246-1
- 30 TABLET in 1 BOTTLE, PLASTIC (68788-9246-3) · 68788-9246-3
- 60 TABLET in 1 BOTTLE, PLASTIC (68788-9246-6) · 68788-9246-6
- 120 TABLET in 1 BOTTLE, PLASTIC (68788-9246-8) · 68788-9246-8
- 90 TABLET in 1 BOTTLE, PLASTIC (68788-9246-9) · 68788-9246-9
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 →