NDC 85509-1435 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC85509-1435

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
PHOENIX RX LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204770
Marketed since
November 22, 2016
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
85509-1435-1120 TABLET in 1 BOTTLE (85509-1435-1)Oct 16, 2025
85509-1435-330 TABLET in 1 BOTTLE (85509-1435-3)Oct 16, 2025
85509-1435-660 TABLET in 1 BOTTLE (85509-1435-6)Oct 16, 2025
85509-1435-990 TABLET in 1 BOTTLE (85509-1435-9)Oct 16, 2025

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