FDA.reportPublic FDA data

CHILDRENS IBUPROFEN

Product NDC
58602-003
11-digit product format
586020003
Labeler code
58602
Product ID
58602-003_317fdce4-a082-4e9a-85b8-380ab68a6631
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Aurohealth LLC
Application
ANDA209179
Marketing category
ANDA
Marketing start
2021-06-16
Substance
IBUPROFEN
Active strength
100 mg/5mL
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
CHILDRENS IBUPROFEN
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IBUPROFEN100 mg/5mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWK2XYI10QM
Rxcui197803

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
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
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
58602-003-20CHILDRENS IBUPROFEN1 in 1 CARTONSUSPENSION12
58602-003-20CHILDRENS IBUPROFEN240 mL in 1 BOTTLESUSPENSION2402
58602-003-24CHILDRENS IBUPROFEN120 mL in 1 BOTTLESUSPENSION1202
58602-003-24CHILDRENS IBUPROFEN1 in 1 CARTONSUSPENSION12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58602-003CHILDRENS IBUPROFEN (IBUPROFEN) SUSPENSION [AUROHEALTH LLC]1Current NDC, Legacy NDC, 4 package rows20210624_0e1bcb06-be48-4efc-82e2-516582e02348.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197803ibuprofen 100 MG in 5 mL Oral SuspensionPSN0e1bcb06-be48-4efc-82e2-516582e023482
197803ibuprofen 20 MG/ML Oral SuspensionSCD0e1bcb06-be48-4efc-82e2-516582e023482
197803ibuprofen 100 MG per 5 ML Oral SuspensionSY0e1bcb06-be48-4efc-82e2-516582e023482
197803ibuprofen 200 MG per 10 ML Oral SuspensionSY0e1bcb06-be48-4efc-82e2-516582e023482

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
58602-003-20586020003201 BOTTLE in 1 CARTON (58602-003-20) / 240 mL in 1 BOTTLE1 bottle2021-06-160000-00-00NoNoCurrent
58602-003-24586020003241 BOTTLE in 1 CARTON (58602-003-24) / 120 mL in 1 BOTTLE1 bottle2021-06-160000-00-00NoNoCurrent