NDC 71335-2066 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2066

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204770
Marketed since
November 22, 2016
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2066-130 TABLET in 1 BOTTLE (71335-2066-1)Nov 10, 2023
71335-2066-290 TABLET in 1 BOTTLE (71335-2066-2)Apr 2, 2024
71335-2066-3100 TABLET in 1 BOTTLE (71335-2066-3)Aug 12, 2024
71335-2066-460 TABLET in 1 BOTTLE (71335-2066-4)Mar 18, 2022
71335-2066-510 TABLET in 1 BOTTLE (71335-2066-5)Aug 12, 2024
71335-2066-620 TABLET in 1 BOTTLE (71335-2066-6)Aug 12, 2024
71335-2066-7120 TABLET in 1 BOTTLE (71335-2066-7)Aug 12, 2024
71335-2066-815 TABLET in 1 BOTTLE (71335-2066-8)Aug 12, 2024

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