NDC 71335-1796 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1796

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212378
Marketed since
October 14, 2020
Listing expires
December 31, 2027
Pharmacologic class
gamma-Aminobutyric Acid-ergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Baclofen →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1796-0120 TABLET in 1 BOTTLE (71335-1796-0)Dec 20, 2021
71335-1796-190 TABLET in 1 BOTTLE (71335-1796-1)Dec 20, 2021
71335-1796-220 TABLET in 1 BOTTLE (71335-1796-2)Dec 20, 2021
71335-1796-360 TABLET in 1 BOTTLE (71335-1796-3)Dec 20, 2021
71335-1796-445 TABLET in 1 BOTTLE (71335-1796-4)Dec 20, 2021
71335-1796-5112 TABLET in 1 BOTTLE (71335-1796-5)Dec 20, 2021
71335-1796-630 TABLET in 1 BOTTLE (71335-1796-6)Dec 20, 2021
71335-1796-756 TABLET in 1 BOTTLE (71335-1796-7)Dec 20, 2021
71335-1796-815 TABLET in 1 BOTTLE (71335-1796-8)Dec 20, 2021
71335-1796-984 TABLET in 1 BOTTLE (71335-1796-9)Dec 20, 2021

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