NDC 71335-1356 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1356

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211659
Marketed since
December 6, 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
71335-1356-0120 TABLET in 1 BOTTLE (71335-1356-0)Mar 17, 2020
71335-1356-190 TABLET in 1 BOTTLE (71335-1356-1)Nov 13, 2019
71335-1356-220 TABLET in 1 BOTTLE (71335-1356-2)Sep 5, 2024
71335-1356-360 TABLET in 1 BOTTLE (71335-1356-3)Dec 6, 2019
71335-1356-445 TABLET in 1 BOTTLE (71335-1356-4)Sep 5, 2024
71335-1356-5112 TABLET in 1 BOTTLE (71335-1356-5)Sep 5, 2024
71335-1356-630 TABLET in 1 BOTTLE (71335-1356-6)Apr 20, 2020
71335-1356-756 TABLET in 1 BOTTLE (71335-1356-7)Sep 5, 2024
71335-1356-815 TABLET in 1 BOTTLE (71335-1356-8)Sep 5, 2024
71335-1356-984 TABLET in 1 BOTTLE (71335-1356-9)Sep 5, 2024

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