Nabumetone

Product NDC
68788-7597
11-digit product format
687887597
Labeler code
68788
Product ID
68788-7597_1f953669-46a2-42c0-999e-60f78dc641c8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nabumetone
Dosage form
TABLET
Route
ORAL
Labeler
Preferred Pharmaceuticals Inc.
Application
ANDA078420
Marketing category
ANDA
Marketing start
2020-02-13
Substance
NABUMETONE
Active strength
750 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

Additional Listing Data#

Finished product
Yes
Brand name base
Nabumetone
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
NABUMETONE750 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiLW0TIW155Z
Rxcui311893

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
9d4d18c4-d38e-37e1-df1c-ee38762bf8a5Product name420251024

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68788-7597-1Nabumetone100 in 1 BOTTLETABLET1005
68788-7597-2Nabumetone20 in 1 BOTTLETABLET205
68788-7597-3Nabumetone30 in 1 BOTTLETABLET305
68788-7597-6Nabumetone60 in 1 BOTTLETABLET605
68788-7597-8Nabumetone120 in 1 BOTTLETABLET1205
68788-7597-9Nabumetone90 in 1 BOTTLETABLET905

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68788-7597-1EA - Each68788-75973c78549b-cde7-45f0-b6de-2082e8ab3fe012020-04-20
68788-7597-2EA - Each68788-759753007ca8-c0cf-4b9e-a6c6-cc7fa3ff87b912020-04-20
68788-7597-3EA - Each68788-7597337e5ec1-726a-40a6-9ce9-93be59c696de12020-04-20
68788-7597-6EA - Each68788-7597e46d173b-a9af-4e40-89e0-b3a8d264e28b12020-04-20
68788-7597-8EA - Each68788-7597380bbafe-ff15-4103-8543-d812f3a4ef8712020-04-20
68788-7597-9EA - Each68788-7597326542ea-164a-467d-a0c8-259933e3ae5012020-04-20

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68788-7597NABUMETONE TABLET [PREFERRED PHARMACEUTICALS INC.]4Current NDC, Legacy NDC, 6 package rows20240724_455c9992-39a0-4353-a121-57e700c77942.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311893nabumetone 750 MG Oral TabletPSN455c9992-39a0-4353-a121-57e700c779425
311893nabumetone 750 MG Oral TabletSCD455c9992-39a0-4353-a121-57e700c779425

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68788-7597-168788759701100 TABLET in 1 BOTTLE (68788-7597-1) 100 tablet2020-02-130000-00-00NoNoCurrent
68788-7597-26878875970220 TABLET in 1 BOTTLE (68788-7597-2) 20 tablet2020-02-130000-00-00NoNoCurrent
68788-7597-36878875970330 TABLET in 1 BOTTLE (68788-7597-3) 30 tablet2020-02-130000-00-00NoNoCurrent
68788-7597-66878875970660 TABLET in 1 BOTTLE (68788-7597-6) 60 tablet2020-02-130000-00-00NoNoCurrent
68788-7597-868788759708120 TABLET in 1 BOTTLE (68788-7597-8) 120 tablet2020-02-130000-00-00NoNoCurrent
68788-7597-96878875970990 TABLET in 1 BOTTLE (68788-7597-9) 90 tablet2020-02-130000-00-00NoNoCurrent