NDC 0591-3670 – Nabumetone

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

Human Prescription Drug

Product NDC0591-3670

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091083
Marketed since
June 13, 2011
Listing expires
December 31, 2026
Pharmacologic class
Nonsteroidal Anti-inflammatory Drug

Active ingredients

Uses, dosage, side effects and warnings for Nabumetone →

Package NDC codes (2)

Package NDCDescriptionSince
0591-3670-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3670-01)Jun 13, 2011
0591-3670-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3670-05)Jun 13, 2011

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