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
- 84386-035_f4e8cbc5-b1f2-4331-a267-d5bd90bcde8a
- Product NDC
- 84386-035
- Form
- TABLET
- Composition / generic term
- BACLOFEN
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251121
- Source listing expiry
- 20261231
Source-listed ingredients
- BACLOFEN — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (84386-035-01) · 84386-035-01
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 →