NDC 50228-323 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50228-323

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
ScieGen Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207466
Marketed since
August 31, 2017
Listing expires
December 31, 2026
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (3)

Package NDCDescriptionSince
50228-323-01100 TABLET in 1 BOTTLE (50228-323-01)Aug 31, 2017
50228-323-05500 TABLET in 1 BOTTLE (50228-323-05)Aug 31, 2017
50228-323-3030 TABLET in 1 BOTTLE (50228-323-30)Aug 31, 2017

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