NDC 70954-785 – Nabumetone

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

Human Prescription Drug

Product NDC70954-785

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA219118
Marketed since
January 7, 2025
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (2)

Package NDCDescriptionSince
70954-785-10100 TABLET, FILM COATED in 1 BOTTLE (70954-785-10)Jan 7, 2025
70954-785-20500 TABLET, FILM COATED in 1 BOTTLE (70954-785-20)Jan 7, 2025

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