NDC 51655-396 – Nabumetone

Nabumetone 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51655-396

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078671
Marketed since
July 7, 2020
Listing expires
December 31, 2027
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (1)

Package NDCDescriptionSince
51655-396-2560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-396-25)Jul 7, 2020

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