NDC 85509-2341 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC85509-2341

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
PHOENIX RX LLC
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 (5)

Package NDCDescriptionSince
85509-2341-1100 TABLET in 1 BOTTLE (85509-2341-1)Jul 31, 2025
85509-2341-2120 TABLET in 1 BOTTLE (85509-2341-2)Jul 31, 2025
85509-2341-330 TABLET in 1 BOTTLE (85509-2341-3)Jul 31, 2025
85509-2341-660 TABLET in 1 BOTTLE (85509-2341-6)Jul 31, 2025
85509-2341-990 TABLET in 1 BOTTLE (85509-2341-9)Jul 31, 2025

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