NDC 71335-2497 – Baclofen

Baclofen 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2497

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA214374
Marketed since
March 1, 2024
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
71335-2497-0120 TABLET in 1 BOTTLE (71335-2497-0)Sep 16, 2024
71335-2497-190 TABLET in 1 BOTTLE (71335-2497-1)Sep 16, 2024
71335-2497-220 TABLET in 1 BOTTLE (71335-2497-2)Sep 16, 2024
71335-2497-360 TABLET in 1 BOTTLE (71335-2497-3)Sep 16, 2024
71335-2497-445 TABLET in 1 BOTTLE (71335-2497-4)Sep 16, 2024
71335-2497-5112 TABLET in 1 BOTTLE (71335-2497-5)Sep 16, 2024
71335-2497-630 TABLET in 1 BOTTLE (71335-2497-6)Sep 16, 2024
71335-2497-756 TABLET in 1 BOTTLE (71335-2497-7)Sep 16, 2024
71335-2497-815 TABLET in 1 BOTTLE (71335-2497-8)Sep 16, 2024
71335-2497-984 TABLET in 1 BOTTLE (71335-2497-9)Sep 16, 2024

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