NDC 71335-0103 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0103

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077241
Marketed since
December 20, 2005
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
71335-0103-0120 TABLET in 1 BOTTLE (71335-0103-0)Mar 6, 2018
71335-0103-190 TABLET in 1 BOTTLE (71335-0103-1)Feb 15, 2018
71335-0103-220 TABLET in 1 BOTTLE (71335-0103-2)Dec 27, 2021
71335-0103-360 TABLET in 1 BOTTLE (71335-0103-3)Feb 12, 2018
71335-0103-445 TABLET in 1 BOTTLE (71335-0103-4)Dec 27, 2021
71335-0103-5112 TABLET in 1 BOTTLE (71335-0103-5)Dec 27, 2021
71335-0103-630 TABLET in 1 BOTTLE (71335-0103-6)Feb 26, 2018
71335-0103-756 TABLET in 1 BOTTLE (71335-0103-7)Dec 27, 2021
71335-0103-815 TABLET in 1 BOTTLE (71335-0103-8)Dec 27, 2021
71335-0103-984 TABLET in 1 BOTTLE (71335-0103-9)Dec 27, 2021

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