FDA.reportPublic FDA data

Ibuprofen

Product NDC
55910-791
11-digit product format
559100791
Labeler code
55910
Product ID
55910-791_ab690460-e705-4a04-a047-acaf76aa9aca
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
DOLGENCORP, LLC
Application
ANDA075010
Marketing category
ANDA
Marketing start
2023-05-12
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
55910-791-08Ibuprofen1 in 1 CARTONTABLET, FILM COATED14
55910-791-08Ibuprofen24 in 1 BOTTLE, PLASTICTABLET, FILM COATED244
55910-791-96Ibuprofen100 in 1 BOTTLE, PLASTICTABLET, FILM COATED1004
55910-791-96Ibuprofen2 in 1 CARTONTABLET, FILM COATED24

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55910-791IBUPROFEN TABLET, FILM COATED [DOLGENCORP, LLC]3Current NDC, 4 package rows20250105_37ccb303-c70e-48b3-a8a3-2b0097cf8f88.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSN37ccb303-c70e-48b3-a8a3-2b0097cf8f884
310965ibuprofen 200 MG Oral TabletSCD37ccb303-c70e-48b3-a8a3-2b0097cf8f884
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY37ccb303-c70e-48b3-a8a3-2b0097cf8f884

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
55910-791-08559100791081 BOTTLE, PLASTIC in 1 CARTON (55910-791-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2023-05-12NoNoCurrent
55910-791-96559100791962 BOTTLE, PLASTIC in 1 CARTON (55910-791-96) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC2023-05-12NoNoCurrent