Nabumetone

Product NDC
71205-977
11-digit product format
712050977
Labeler code
71205
Product ID
71205-977_40ce485f-575c-4c51-8058-83b10a8ddac7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nabumetone
Dosage form
TABLET
Route
ORAL
Labeler
Proficient Rx LP
Application
ANDA078420
Marketing category
ANDA
Marketing start
2019-09-25
Substance
NABUMETONE
Active strength
500 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
LW0TIW155ZNABUMETONE42924-53-8NABUMETONE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71205-977-0071205097700100 TABLET in 1 BOTTLE, PLASTIC (71205-977-00) 100 tablet2020-05-07NoNoHistorical
71205-977-307120509773030 TABLET in 1 BOTTLE, PLASTIC (71205-977-30) 30 tablet2020-05-07NoNoHistorical
71205-977-5571205097755500 TABLET in 1 BOTTLE, PLASTIC (71205-977-55) 500 tablet2020-05-07NoNoHistorical
71205-977-607120509776060 TABLET in 1 BOTTLE, PLASTIC (71205-977-60) 60 tablet2020-05-07NoNoHistorical
71205-977-7271205097772120 TABLET in 1 BOTTLE, PLASTIC (71205-977-72) 120 tablet2020-05-07NoNoHistorical
71205-977-907120509779090 TABLET in 1 BOTTLE, PLASTIC (71205-977-90) 90 tablet2020-05-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
NABUMETONE TABLETS USPProficient Rx LP2022-05-01HUMAN PRESCRIPTION DRUG LABEL3