Nabumetone

Product NDC

70518-0934

11-digit product format

705180934

Labeler code

70518

Product ID

70518-0934_a5b41746-7907-495e-e053-2995a90a9cb9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumetone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA078671

Marketing category

ANDA

Marketing start

2018-01-05

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

2021-12-31

Current FDA listing

Historical FDA.report record