NDC 0527-1435 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0527-1435

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Lannett Company, Inc.
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 (2)

Package NDCDescriptionSince
0527-1435-01100 TABLET in 1 BOTTLE (0527-1435-01)Nov 22, 2016
0527-1435-05500 TABLET in 1 BOTTLE (0527-1435-05)Nov 22, 2016

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