NDC 79739-7077 – Nabumetone 750 mg

Nabumetone 750 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC79739-7077

Product details

Brand name
Nabumetone 750 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

Uses, dosage, side effects and warnings for Nabumetone 750 mg →

Package NDC codes (2)

Package NDCDescriptionSince
79739-7077-1100 TABLET, FILM COATED in 1 BOTTLE (79739-7077-1)Sep 4, 2019
79739-7077-5500 TABLET, FILM COATED in 1 BOTTLE (79739-7077-5)Sep 4, 2019