NDC 71335-2756 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2756

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212067
Marketed since
July 9, 2020
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
71335-2756-0120 TABLET in 1 BOTTLE (71335-2756-0)Oct 3, 2025
71335-2756-190 TABLET in 1 BOTTLE (71335-2756-1)Oct 3, 2025
71335-2756-220 TABLET in 1 BOTTLE (71335-2756-2)Oct 3, 2025
71335-2756-360 TABLET in 1 BOTTLE (71335-2756-3)Oct 3, 2025
71335-2756-445 TABLET in 1 BOTTLE (71335-2756-4)Oct 3, 2025
71335-2756-5112 TABLET in 1 BOTTLE (71335-2756-5)Oct 3, 2025
71335-2756-630 TABLET in 1 BOTTLE (71335-2756-6)Oct 3, 2025
71335-2756-756 TABLET in 1 BOTTLE (71335-2756-7)Oct 3, 2025
71335-2756-815 TABLET in 1 BOTTLE (71335-2756-8)Oct 3, 2025
71335-2756-984 TABLET in 1 BOTTLE (71335-2756-9)Oct 3, 2025

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