Nabumetone

Product NDC

35356-686

11-digit product format

353560686

Labeler code

35356

Product ID

35356-686_fe46e1b0-1fc7-42b5-b49c-bb17c818cec7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumetone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC

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