NDC 71205-016 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-016

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207466
Marketed since
August 31, 2017
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (4)

Package NDCDescriptionSince
71205-016-1010 TABLET in 1 BOTTLE (71205-016-10)Apr 2, 2018
71205-016-3030 TABLET in 1 BOTTLE (71205-016-30)Apr 2, 2018
71205-016-6060 TABLET in 1 BOTTLE (71205-016-60)Apr 2, 2018
71205-016-9090 TABLET in 1 BOTTLE (71205-016-90)Apr 2, 2018

Other Metaxalone products