FDA.reportPublic FDA data

ibuprofen

Product NDC
41250-647
11-digit product format
412500647
Labeler code
41250
Product ID
41250-647_27661b00-42d1-4f86-8c56-04cfece82d4f
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Meijer Distribution Inc
Application
ANDA072096
Marketing category
ANDA
Marketing start
1988-11-15
Substance
IBUPROFEN
Active strength
200 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
ibuprofen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IBUPROFEN200 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWK2XYI10QM
Rxcui310965

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41250-647-71ibuprofen50 in 1 BOTTLETABLET, FILM COATED508
41250-647-71ibuprofen1 in 1 CARTONTABLET, FILM COATED18
41250-647-76ibuprofen120 in 1 BOTTLETABLET, FILM COATED1208
41250-647-76ibuprofen1 in 1 CARTONTABLET, FILM COATED18
41250-647-78ibuprofen1 in 1 CARTONTABLET, FILM COATED18
41250-647-78ibuprofen100 in 1 BOTTLETABLET, FILM COATED1008
41250-647-82ibuprofen2 in 1 CARTONTABLET, FILM COATED28
41250-647-82ibuprofen100 in 1 BOTTLETABLET, FILM COATED1008
41250-647-90ibuprofen500 in 1 BOTTLETABLET, FILM COATED5008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-647IBUPROFEN TABLET, FILM COATED [MEIJER DISTRIBUTION INC]8Current NDC, Legacy NDC, 9 package rows20250507_66b19ed1-6cf9-4705-82cd-02f23c6379e7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSN66b19ed1-6cf9-4705-82cd-02f23c6379e78
310965ibuprofen 200 MG Oral TabletSCD66b19ed1-6cf9-4705-82cd-02f23c6379e78
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY66b19ed1-6cf9-4705-82cd-02f23c6379e78

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41250-647-71412500647711 BOTTLE in 1 CARTON (41250-647-71) / 50 TABLET, FILM COATED in 1 BOTTLE1 bottle1988-11-150000-00-00NoNoCurrent
41250-647-76412500647761 BOTTLE in 1 CARTON (41250-647-76) > 120 TABLET, FILM COATED in 1 BOTTLE1 bottle1992-04-170000-00-00NoNoCurrent
41250-647-78412500647781 BOTTLE in 1 CARTON (41250-647-78) / 100 TABLET, FILM COATED in 1 BOTTLE1 bottle1991-09-200000-00-00NoNoCurrent
41250-647-82412500647822 BOTTLE in 1 CARTON (41250-647-82) / 100 TABLET, FILM COATED in 1 BOTTLE2 bottle2016-09-020000-00-00NoNoCurrent
41250-647-9041250064790500 TABLET, FILM COATED in 1 BOTTLE (41250-647-90) 1994-09-070000-00-00NoNoCurrent