Nabumetone

Product NDC
50090-5386
11-digit product format
500905386
Labeler code
50090
Product ID
50090-5386_b14d72e2-bd9d-4c5c-ba28-c738e129284f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nabumetone
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA078671
Marketing category
ANDA
Marketing start
2019-03-06
Marketing end
0000-00-00
Substance
NABUMETONE
Active strength
750 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-5386-0EA - Each50090-53861fc50492-e233-4231-a97d-54990a9ac56112023-03-13
50090-5386-2EA - Each50090-538685a60fab-b7bd-454c-8688-51c105e6b87812023-03-13
50090-5386-3EA - Each50090-53860aa8843d-4fbb-4929-8985-0bd7a996881712023-03-13
50090-5386-4EA - Each50090-5386d12d03a9-49a4-4811-b333-fe0b2fbe8d7012023-03-13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-5386-05009053860030 TABLET, FILM COATED in 1 BOTTLE (50090-5386-0) 2020-11-200000-00-00NoNoCurrent
50090-5386-25009053860214 TABLET, FILM COATED in 1 BOTTLE (50090-5386-2) 2020-11-200000-00-00NoNoCurrent
50090-5386-35009053860360 TABLET, FILM COATED in 1 BOTTLE (50090-5386-3) 2020-11-200000-00-00NoNoCurrent
50090-5386-45009053860420 TABLET, FILM COATED in 1 BOTTLE (50090-5386-4) 2020-11-200000-00-00NoNoCurrent