NDC 71335-2668 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2668

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 (10)

Package NDCDescriptionSince
71335-2668-0120 TABLET in 1 BOTTLE (71335-2668-0)Jul 15, 2025
71335-2668-190 TABLET in 1 BOTTLE (71335-2668-1)Jul 15, 2025
71335-2668-220 TABLET in 1 BOTTLE (71335-2668-2)Jul 15, 2025
71335-2668-360 TABLET in 1 BOTTLE (71335-2668-3)Jul 15, 2025
71335-2668-445 TABLET in 1 BOTTLE (71335-2668-4)Jul 15, 2025
71335-2668-5112 TABLET in 1 BOTTLE (71335-2668-5)Jul 15, 2025
71335-2668-630 TABLET in 1 BOTTLE (71335-2668-6)Jul 15, 2025
71335-2668-756 TABLET in 1 BOTTLE (71335-2668-7)Jul 15, 2025
71335-2668-815 TABLET in 1 BOTTLE (71335-2668-8)Jul 15, 2025
71335-2668-984 TABLET in 1 BOTTLE (71335-2668-9)Jul 15, 2025

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