IBU

Product NDC
50436-0684
11-digit product format
504360684
Labeler code
50436
Product ID
50436-0684_97aeb9d2-7f81-4db3-b2d3-d238af2adac7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
Unit Dose Services
Application
ANDA075682
Marketing category
ANDA
Marketing start
2008-11-20
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
800 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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015Product name420230808
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
61c18d4e-b552-5478-8fc0-df38b93e3100Product name120140508
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
997601aa-bb5f-6971-6b90-a21132c12c7bProduct name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50436-0684-1IBU30 in 1 BOTTLETABLET305
50436-0684-2IBU60 in 1 BOTTLETABLET605
50436-0684-3IBU90 in 1 BOTTLETABLET905
50436-0684-4IBU10 in 1 BOTTLETABLET105
50436-0684-5IBU12 in 1 BOTTLETABLET125
50436-0684-6IBU15 in 1 BOTTLETABLET155

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
IbuprofenACTIVE INGREDIENTWK2XYI10QMIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
IbuprofenACTIVE MOIETYWK2XYI10QMIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
carnauba waxINACTIVE INGREDIENTR12CBM0EIZIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
cellulose, microcrystallineINACTIVE INGREDIENTOP1R32D61UIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
croscarmellose sodiumINACTIVE INGREDIENTM28OL1HH48IBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
hypromellosesINACTIVE INGREDIENT3NXW29V3WOIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
magnesium stearateINACTIVE INGREDIENT70097M6I30IBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
polydextroseINACTIVE INGREDIENTVH2XOU12IEIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
Polyethylene glycolsINACTIVE INGREDIENT3WJQ0SDW1AIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
polysorbate 80INACTIVE INGREDIENT6OZP39ZG8HIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
silicon dioxideINACTIVE INGREDIENTETJ7Z6XBU4IBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2
titanium dioxideINACTIVE INGREDIENT15FIX9V2JPIBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50436-0684IBU (IBUPROFEN) TABLET [UNIT DOSE SERVICES]5Legacy NDC, 6 package rows20180110_bf56640a-3f81-4166-8f0f-f45a26e6545b.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
206905Ibu 400 MG Oral TabletPSNbf56640a-3f81-4166-8f0f-f45a26e6545b5
206917Ibu 800 MG Oral TabletPSNbf56640a-3f81-4166-8f0f-f45a26e6545b5
197805ibuprofen 400 MG Oral TabletPSNbf56640a-3f81-4166-8f0f-f45a26e6545b5
197807ibuprofen 800 MG Oral TabletPSNbf56640a-3f81-4166-8f0f-f45a26e6545b5
206905ibuprofen 400 MG Oral Tablet [Ibu]SBDbf56640a-3f81-4166-8f0f-f45a26e6545b5
206917ibuprofen 800 MG Oral Tablet [Ibu]SBDbf56640a-3f81-4166-8f0f-f45a26e6545b5
197805ibuprofen 400 MG Oral TabletSCDbf56640a-3f81-4166-8f0f-f45a26e6545b5
197807ibuprofen 800 MG Oral TabletSCDbf56640a-3f81-4166-8f0f-f45a26e6545b5
206905Ibu 400 MG Oral TabletSYbf56640a-3f81-4166-8f0f-f45a26e6545b5
206917Ibu 800 MG Oral TabletSYbf56640a-3f81-4166-8f0f-f45a26e6545b5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
50436-0684-15043606840130 in 1 BOTTLEHistorical
50436-0684-25043606840260 in 1 BOTTLEHistorical
50436-0684-35043606840390 in 1 BOTTLEHistorical
50436-0684-45043606840410 in 1 BOTTLEHistorical
50436-0684-55043606840512 in 1 BOTTLEHistorical
50436-0684-65043606840615 in 1 BOTTLEHistorical