Nabumetone

Product NDC

0615-7667

11-digit product format

006157667

Labeler code

0615

Product ID

0615-7667_54a6ebca-d297-4ebe-b9b0-0c8d2b446a77

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumetone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA075189

Marketing category

ANDA

Marketing start

2010-01-22

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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record