NDC 68788-7675 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68788-7675

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA204770
Marketed since
March 2, 2020
Listing expires
December 31, 2027
Pharmacologic class
Muscle Relaxant

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (6)

Package NDCDescriptionSince
68788-7675-015 TABLET in 1 BOTTLE (68788-7675-0)Mar 2, 2020
68788-7675-1100 TABLET in 1 BOTTLE (68788-7675-1)Mar 2, 2020
68788-7675-220 TABLET in 1 BOTTLE (68788-7675-2)Mar 2, 2020
68788-7675-330 TABLET in 1 BOTTLE (68788-7675-3)Mar 2, 2020
68788-7675-660 TABLET in 1 BOTTLE (68788-7675-6)Mar 2, 2020
68788-7675-990 TABLET in 1 BOTTLE (68788-7675-9)Mar 2, 2020

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