FDA.reportPublic FDA data

Ibuprofen

Product NDC
41250-293
11-digit product format
412500293
Labeler code
41250
Product ID
41250-293_30a3cb82-e3eb-24d4-e063-6394a90aa84b
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
MEIJER DISTRIBUTION INC.
Application
ANDA078682
Marketing category
ANDA
Marketing start
2020-03-19
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
Rxcui310964

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
41250-293-15Ibuprofen1 in 1 CARTONCAPSULE, LIQUID FILLED14
41250-293-15Ibuprofen40 in 1 BOTTLECAPSULE, LIQUID FILLED404
41250-293-78Ibuprofen1 in 1 CARTONCAPSULE, LIQUID FILLED14
41250-293-78Ibuprofen80 in 1 BOTTLECAPSULE, LIQUID FILLED804
41250-293-79Ibuprofen160 in 1 BOTTLECAPSULE, LIQUID FILLED1604
41250-293-83Ibuprofen300 in 1 BOTTLECAPSULE, LIQUID FILLED3004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41250-293IBUPROFEN CAPSULE, LIQUID FILLED [MEIJER DISTRIBUTION INC.]4Current NDC, Legacy NDC, 6 package rows20250322_a13ac87b-b395-685e-e053-2a95a90ab5d3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310964ibuprofen 200 MG Oral CapsulePSNa13ac87b-b395-685e-e053-2a95a90ab5d34
310964ibuprofen 200 MG Oral CapsuleSCDa13ac87b-b395-685e-e053-2a95a90ab5d34

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41250-293-15412500293151 BOTTLE in 1 CARTON (41250-293-15) / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2020-03-190000-00-00NoNoCurrent
41250-293-78412500293781 BOTTLE in 1 CARTON (41250-293-78) / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2020-03-190000-00-00NoNoCurrent
41250-293-7941250029379160 CAPSULE, LIQUID FILLED in 1 BOTTLE (41250-293-79) 2020-03-190000-00-00NoNoCurrent
41250-293-8341250029383300 CAPSULE, LIQUID FILLED in 1 BOTTLE (41250-293-83) 2020-03-190000-00-00NoNoCurrent