NDC 69306-100 – Metaxalone

Metaxalone 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69306-100

Product details

Brand name
Metaxalone
Generic name
Metaxalone
Labeler
Doc Rx
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203695
Marketed since
April 1, 2019
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Metaxalone →

Package NDC codes (6)

Package NDCDescriptionSince
69306-100-01100 TABLET in 1 BOTTLE (69306-100-01)Apr 1, 2019
69306-100-0220 TABLET in 1 BOTTLE (69306-100-02)Jan 1, 2020
69306-100-0330 TABLET in 1 BOTTLE (69306-100-03)Dec 13, 2019
69306-100-0660 TABLET in 1 BOTTLE (69306-100-06)Dec 13, 2019
69306-100-0990 TABLET in 1 BOTTLE (69306-100-09)Dec 13, 2019
69306-100-1515 TABLET in 1 BOTTLE (69306-100-15)Jan 1, 2020

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