NDC 71335-2219 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2219

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214099
Marketed since
July 13, 2021
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
71335-2219-0120 TABLET in 1 BOTTLE (71335-2219-0)Aug 15, 2023
71335-2219-190 TABLET in 1 BOTTLE (71335-2219-1)Aug 15, 2023
71335-2219-220 TABLET in 1 BOTTLE (71335-2219-2)Aug 15, 2023
71335-2219-360 TABLET in 1 BOTTLE (71335-2219-3)Aug 15, 2023
71335-2219-445 TABLET in 1 BOTTLE (71335-2219-4)Aug 15, 2023
71335-2219-5112 TABLET in 1 BOTTLE (71335-2219-5)Aug 15, 2023
71335-2219-630 TABLET in 1 BOTTLE (71335-2219-6)Aug 15, 2023
71335-2219-756 TABLET in 1 BOTTLE (71335-2219-7)Aug 15, 2023
71335-2219-815 TABLET in 1 BOTTLE (71335-2219-8)Aug 15, 2023
71335-2219-984 TABLET in 1 BOTTLE (71335-2219-9)Aug 15, 2023

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