NDC 71205-326 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-326

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Proficient Rx LP
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 (4)

Package NDCDescriptionSince
71205-326-2020 TABLET in 1 BOTTLE (71205-326-20)Sep 30, 2020
71205-326-3030 TABLET in 1 BOTTLE (71205-326-30)Sep 1, 2019
71205-326-6060 TABLET in 1 BOTTLE (71205-326-60)Sep 1, 2019
71205-326-9090 TABLET in 1 BOTTLE (71205-326-90)Sep 1, 2019

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