NDC 79739-7078 – Nabumetone 1000 mg

Nabumetone 1000 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC79739-7078

Product details

Brand name
Nabumetone 1000 mg
Generic name
Nabumetone
Labeler
LGM PHARMA SOLUTIONS, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203166
Marketed since
September 4, 2019
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Package NDC codes (3)

Package NDCDescriptionSince
79739-7078-1100 TABLET, FILM COATED in 1 BOTTLE (79739-7078-1)Sep 4, 2019
79739-7078-330 TABLET, FILM COATED in 1 BOTTLE (79739-7078-3)Oct 2, 2019
79739-7078-660 TABLET, FILM COATED in 1 BOTTLE (79739-7078-6)Jul 24, 2020