FDA.reportPublic FDA data

Ibuprofen

Product NDC
21130-358
11-digit product format
211300358
Labeler code
21130
Product ID
21130-358_463f0f46-f34e-3415-e063-6394a90aa40f
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
BETTER LIVING BRANDS LLC.
Application
ANDA202312
Marketing category
ANDA
Marketing start
2019-07-12
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
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
21130-358-052020-08-04C16284748780-1ab0e2407-2fb7-f274-e053-dbdaa90a6471Ibuprofen Tablets USP, 200 mg Pain Reliever/Fever Reducer (NSAID)* See New Warnings
21130-358-502020-08-04C16284748780-1ab0e2407-2fb7-f274-e053-dbdaa90a6471Ibuprofen Tablets USP, 200 mg Pain Reliever/Fever Reducer (NSAID)* See New Warnings
21130-358-052020-07-22C16284748780-1ab0e2407-2fb7-f274-e053-dbdaa90a6471Ibuprofen Tablets USP, 200 mg Pain Reliever/Fever Reducer (NSAID)* See New Warnings
21130-358-502020-07-22C16284748780-1ab0e2407-2fb7-f274-e053-dbdaa90a6471Ibuprofen Tablets USP, 200 mg Pain Reliever/Fever Reducer (NSAID)* See New Warnings

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
21130-358-05Ibuprofen50 in 1 BOTTLETABLET, COATED507
21130-358-10Ibuprofen100 in 1 BOTTLETABLET, COATED1007
21130-358-50Ibuprofen500 in 1 BOTTLETABLET, COATED5007

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
21130-358IBUPROFEN TABLET, COATED [BETTER LIVING BRANDS LLC.]6Current NDC, Legacy NDC, 3 package rows20241212_a3c1a61b-88fc-419c-e053-2a95a90ac0c3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSNa3c1a61b-88fc-419c-e053-2a95a90ac0c37
310965ibuprofen 200 MG Oral TabletSCDa3c1a61b-88fc-419c-e053-2a95a90ac0c37
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSYa3c1a61b-88fc-419c-e053-2a95a90ac0c37

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
21130-358-052113003580550 TABLET, COATED in 1 BOTTLE (21130-358-05) 2019-07-120000-00-00NoNoCurrent
21130-358-1021130035810100 TABLET, COATED in 1 BOTTLE (21130-358-10) 2023-06-30NoNoHistorical
21130-358-5021130035850500 TABLET, COATED in 1 BOTTLE (21130-358-50) 2019-07-120000-00-00NoNoCurrent