Nabumetone

Product NDC

70518-0614

11-digit product format

705180614

Labeler code

70518

Product ID

70518-0614_86431a9a-5b17-c28a-e053-2991aa0a9901

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Nabumentone

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075280

Marketing category

ANDA

Marketing start

2017-07-12

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