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
- 76420-357_3c3b62bc-64f9-f0cb-e063-6394a90a4a92
- Product NDC
- 76420-357
- Form
- TABLET
- Composition / generic term
- BACLOFEN
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180401
- Source listing expiry
- 20261231
Source-listed ingredients
- BACLOFEN — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (76420-357-00) · 76420-357-00
- 100 TABLET in 1 BOTTLE (76420-357-01) · 76420-357-01
- 500 TABLET in 1 BOTTLE (76420-357-05) · 76420-357-05
- 120 TABLET in 1 BOTTLE (76420-357-12) · 76420-357-12
- 30 TABLET in 1 BOTTLE (76420-357-30) · 76420-357-30
- 60 TABLET in 1 BOTTLE (76420-357-60) · 76420-357-60
- 90 TABLET in 1 BOTTLE (76420-357-90) · 76420-357-90
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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