Nabumetone

Product NDC

35356-685

11-digit product format

353560685

Labeler code

35356

Product ID

35356-685_a34aebce-f0b6-4341-8c7f-49bdd1c06fe9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumentone

Dosage form

TABLET

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA075280

Marketing category

ANDA

Marketing start

2002-02-25

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

2020-12-31

Current FDA listing

Historical FDA.report record