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
- 70518-4249_583819cb-334e-fc1f-e063-6394a90a6afe
- Product NDC
- 70518-4249
- Form
- TABLET
- Composition / generic term
- Baclofen
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20241230
- Source listing expiry
- 20271231
Source-listed ingredients
- BACLOFEN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BLISTER PACK (70518-4249-0) · 70518-4249-0
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-4249-1) · 70518-4249-1
- 30 TABLET in 1 BLISTER PACK (70518-4249-2) · 70518-4249-2
- 30 TABLET in 1 BOTTLE, PLASTIC (70518-4249-3) · 70518-4249-3
- 90 TABLET in 1 BOTTLE, PLASTIC (70518-4249-4) · 70518-4249-4
- 14 TABLET in 1 BOTTLE, PLASTIC (70518-4249-5) · 70518-4249-5
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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