NDC 71335-2669 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2669

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212378
Marketed since
June 15, 2024
Listing expires
December 31, 2026
Pharmacologic class
gamma-Aminobutyric Acid-ergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Baclofen →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2669-1100 TABLET in 1 BOTTLE (71335-2669-1)Jun 26, 2025
71335-2669-21000 TABLET in 1 BOTTLE (71335-2669-2)Jun 26, 2025
71335-2669-3120 TABLET in 1 BOTTLE (71335-2669-3)Jun 26, 2025

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