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: 72865-298_2d6876fe-19e5-fd4f-e063-6294a90a7960
Product NDC: 72865-298
Form: TABLET
Composition / generic term: BACLOFEN
Labeler: XLCare Pharmaceuticals Inc.
Marketing category: ANDA
Marketing start / end (source format): 20250205
Source listing expiry: 20261231

Source-listed ingredients

BACLOFEN — 20 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (72865-298-01) · 72865-298-01
500 TABLET in 1 BOTTLE (72865-298-05) · 72865-298-05
1000 TABLET in 1 BOTTLE (72865-298-10) · 72865-298-10

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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