NDC 51655-171 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-171

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207466
Marketed since
July 21, 2022
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (2)

Package NDCDescriptionSince
51655-171-2020 TABLET in 1 BOTTLE, PLASTIC (51655-171-20)Jul 21, 2022
51655-171-5230 TABLET in 1 BOTTLE, PLASTIC (51655-171-52)Feb 3, 2023

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