NDC 76420-232 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76420-232

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Asclemed USA, Inc.
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 (4)

Package NDCDescriptionSince
76420-232-2020 TABLET in 1 BOTTLE (76420-232-20)Jul 25, 2022
76420-232-3030 TABLET in 1 BOTTLE (76420-232-30)Jul 25, 2022
76420-232-6060 TABLET in 1 BOTTLE (76420-232-60)Jul 25, 2022
76420-232-9090 TABLET in 1 BOTTLE (76420-232-90)Jul 25, 2022

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