Nabumetone

Product NDC

66267-529

11-digit product format

662670529

Labeler code

66267

Product ID

66267-529_9cbe8225-1bb5-5528-e053-2995a90adea0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumetone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA078671

Marketing category

ANDA

Marketing start

2008-03-01

Marketing end

0000-00-00

Substance

NABUMETONE

Active strength

750 mg/1

Pharmacologic classes

Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record