NDC 71335-0949 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0949

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209102
Marketed since
April 1, 2018
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
71335-0949-0120 TABLET in 1 BOTTLE (71335-0949-0)Oct 31, 2018
71335-0949-190 TABLET in 1 BOTTLE (71335-0949-1)Sep 11, 2018
71335-0949-220 TABLET in 1 BOTTLE (71335-0949-2)May 29, 2024
71335-0949-360 TABLET in 1 BOTTLE (71335-0949-3)Oct 5, 2018
71335-0949-445 TABLET in 1 BOTTLE (71335-0949-4)May 29, 2024
71335-0949-5112 TABLET in 1 BOTTLE (71335-0949-5)May 29, 2024
71335-0949-630 TABLET in 1 BOTTLE (71335-0949-6)Sep 6, 2018
71335-0949-756 TABLET in 1 BOTTLE (71335-0949-7)May 29, 2024
71335-0949-815 TABLET in 1 BOTTLE (71335-0949-8)May 29, 2024
71335-0949-984 TABLET in 1 BOTTLE (71335-0949-9)May 29, 2024

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