Nabumetone

Product NDC

50436-6334

11-digit product format

504366334

Labeler code

50436

Product ID

50436-6334_97cf6511-89f7-4ce5-a8f2-3b2e7e356963

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumetone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Unit Dose Services

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],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record