NDC 71205-426 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-426

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204770
Marketed since
November 22, 2016
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (5)

Package NDCDescriptionSince
71205-426-1414 TABLET in 1 BOTTLE (71205-426-14)Jan 5, 2022
71205-426-2020 TABLET in 1 BOTTLE (71205-426-20)Jan 5, 2022
71205-426-3030 TABLET in 1 BOTTLE (71205-426-30)Mar 11, 2020
71205-426-6060 TABLET in 1 BOTTLE (71205-426-60)Mar 11, 2020
71205-426-9090 TABLET in 1 BOTTLE (71205-426-90)Mar 11, 2020

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