FDA.reportPublic FDA data

IBUPROFEN

Product NDC
11673-992
11-digit product format
116730992
Labeler code
11673
Product ID
11673-992_0e074882-f7f2-66d4-e063-6394a90ac937
Type
HUMAN OTC DRUG
Nonproprietary name
IBUPROFEN
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
TARGET CORPORATION
Application
ANDA079205
Marketing category
ANDA
Marketing start
2020-01-01
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
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
11673-992-31IBUPROFEN300 in 1 BOTTLECAPSULE, LIQUID FILLED3007
11673-992-44IBUPROFEN40 in 1 BOTTLECAPSULE, LIQUID FILLED407
11673-992-66IBUPROFEN160 in 1 BOTTLECAPSULE, LIQUID FILLED1607
11673-992-66IBUPROFEN1 in 1 CARTONCAPSULE, LIQUID FILLED17
11673-992-80IBUPROFEN80 in 1 BOTTLECAPSULE, LIQUID FILLED807

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-992IBUPROFEN CAPSULE, LIQUID FILLED [TARGET CORPORATION]7Current NDC, Legacy NDC, 5 package rows20240104_8e8646fe-fd62-1662-e053-2a95a90a3008.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310964ibuprofen 200 MG Oral CapsulePSN8e8646fe-fd62-1662-e053-2a95a90a30087
310964ibuprofen 200 MG Oral CapsuleSCD8e8646fe-fd62-1662-e053-2a95a90a30087

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-992-3111673099231300 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-992-31) 2021-03-120000-00-00NoNoCurrent
11673-992-441167309924440 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-992-44) 2020-01-010000-00-00NoNoCurrent
11673-992-66116730992661 BOTTLE in 1 CARTON (11673-992-66) / 160 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2021-03-120000-00-00NoNoCurrent
11673-992-801167309928080 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-992-80) 2020-01-010000-00-00NoNoCurrent