Nabumetone

Product NDC

35356-726

11-digit product format

353560726

Labeler code

35356

Product ID

35356-726_9337c470-89c9-4c7d-bc4a-3734183c1afb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumetone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Lake Erie Medical DBA Quality Care Products LLC

Application

ANDA078671

Marketing category

ANDA

Marketing start

2008-03-01

Marketing end

0000-00-00

Substance

NABUMETONE

Active strength

500 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

2020-12-31

Current FDA listing

Historical FDA.report record