NDC 71335-2392 – Baclofen

Baclofen 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2392

Product details

Brand name
Baclofen
Generic name
Baclofen
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA212067
Marketed since
July 9, 2020
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
71335-2392-0112 TABLET in 1 BOTTLE (71335-2392-0)May 29, 2024
71335-2392-130 TABLET in 1 BOTTLE (71335-2392-1)May 29, 2024
71335-2392-2120 TABLET in 1 BOTTLE (71335-2392-2)May 29, 2024
71335-2392-320 TABLET in 1 BOTTLE (71335-2392-3)May 29, 2024
71335-2392-460 TABLET in 1 BOTTLE (71335-2392-4)May 29, 2024
71335-2392-5100 TABLET in 1 BOTTLE (71335-2392-5)May 29, 2024
71335-2392-656 TABLET in 1 BOTTLE (71335-2392-6)May 29, 2024
71335-2392-790 TABLET in 1 BOTTLE (71335-2392-7)May 29, 2024
71335-2392-8140 TABLET in 1 BOTTLE (71335-2392-8)May 29, 2024
71335-2392-984 TABLET in 1 BOTTLE (71335-2392-9)May 29, 2024

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