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
50090-4682_0825b008-5a6d-4ad7-8cdb-73ebb6692302
Product NDC
50090-4682
Form
TABLET
Composition / generic term
Baclofen
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20181206
Source listing expiry
20271231

Source-listed ingredients

  • BACLOFEN — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 20 TABLET in 1 BOTTLE (50090-4682-0) · 50090-4682-0
  • 60 TABLET in 1 BOTTLE (50090-4682-1) · 50090-4682-1
  • 30 TABLET in 1 BOTTLE (50090-4682-2) · 50090-4682-2
  • 90 TABLET in 1 BOTTLE (50090-4682-3) · 50090-4682-3

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 →