NDC 71335-0375 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0375

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203695
Marketed since
June 19, 2017
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0375-0100 TABLET in 1 BOTTLE (71335-0375-0)Nov 30, 2018
71335-0375-130 TABLET in 1 BOTTLE (71335-0375-1)Nov 30, 2018
71335-0375-220 TABLET in 1 BOTTLE (71335-0375-2)Nov 30, 2018
71335-0375-390 TABLET in 1 BOTTLE (71335-0375-3)Nov 30, 2018
71335-0375-4120 TABLET in 1 BOTTLE (71335-0375-4)Nov 30, 2018
71335-0375-515 TABLET in 1 BOTTLE (71335-0375-5)Nov 30, 2018
71335-0375-610 TABLET in 1 BOTTLE (71335-0375-6)Nov 30, 2018
71335-0375-760 TABLET in 1 BOTTLE (71335-0375-7)Nov 30, 2018
71335-0375-816 TABLET in 1 BOTTLE (71335-0375-8)Nov 30, 2018
71335-0375-984 TABLET in 1 BOTTLE (71335-0375-9)Nov 30, 2018

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