NDC 63187-307 – Nabumetone

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

Human Prescription Drug

Product NDC63187-307

Product details

Brand name
Nabumetone
Generic name
Nabumetone
Labeler
Proficient Rx LP
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 (1)

Package NDCDescriptionSince
63187-307-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-307-30)Jan 1, 2019

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