FDA.reportPublic FDA data

Ibuprofen

Product NDC
41250-993
11-digit product format
412500993
Labeler code
41250
Product ID
41250-993_1335bd3f-e04d-4ea7-b2bf-975c2aaa2b11
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Meijer Distribution Inc
Application
ANDA075139
Marketing category
ANDA
Marketing start
1999-03-01
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Ibuprofen
Listing expiration
2027-12-31

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
41250-993-12Ibuprofen1 in 1 CARTONTABLET, FILM COATED116
41250-993-12Ibuprofen100 in 1 BOTTLETABLET, FILM COATED10016
41250-993-20Ibuprofen225 in 1 BOTTLETABLET, FILM COATED22516
41250-993-91Ibuprofen100 in 1 BOTTLETABLET, FILM COATED10016

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-993IBUPROFEN TABLET, FILM COATED [MEIJER DISTRIBUTION INC]14Current NDC, Legacy NDC, 4 package rows20250428_36f7227d-f3cb-44b7-a4c1-27611cd15052.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSN36f7227d-f3cb-44b7-a4c1-27611cd1505216
310965ibuprofen 200 MG Oral TabletSCD36f7227d-f3cb-44b7-a4c1-27611cd1505216
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY36f7227d-f3cb-44b7-a4c1-27611cd1505216

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
41250-993-12412500993121 in 1 CARTONHistorical
41250-993-2041250099320225 TABLET, FILM COATED in 1 BOTTLE (41250-993-20) 1999-03-010000-00-00NoNoCurrent
41250-993-9141250099391100 TABLET, FILM COATED in 1 BOTTLE (41250-993-91) 1999-03-010000-00-00NoNoCurrent