FDA.reportPublic FDA data

Ibuprofen Oral

Product NDC
72162-1912
11-digit product format
721621912
Labeler code
72162
Product ID
72162-1912_fc73ff4a-ee5d-4415-8c2e-6a2b7079ecb2
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen Oral
Dosage form
SUSPENSION
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA210602
Marketing category
ANDA
Marketing start
2019-09-18
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
Ibuprofen Oral
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
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
72162-1912-2Ibuprofen Oral1 in 1 CARTONSUSPENSION1101
72162-1912-2Ibuprofen Oral118 mL in 1 BOTTLESUSPENSION118101

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1912-2ML - Milliliter72162-1912eac5fec8-dad9-404a-aeeb-4bfe092bc9ba12025-05-14

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1912IBUPROFEN ORAL (IBUPROFEN ORAL) SUSPENSION [BRYANT RANCH PREPACK]101Current NDC, 2 package rows20250223_5c817d24-2dd3-468e-9678-311d038c7b4a.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197803ibuprofen 100 MG in 5 mL Oral SuspensionPSN5c817d24-2dd3-468e-9678-311d038c7b4a101
197803ibuprofen 20 MG/ML Oral SuspensionSCD5c817d24-2dd3-468e-9678-311d038c7b4a101
197803ibuprofen 100 MG per 5 ML Oral SuspensionSY5c817d24-2dd3-468e-9678-311d038c7b4a101
197803ibuprofen 200 MG per 10 ML Oral SuspensionSY5c817d24-2dd3-468e-9678-311d038c7b4a101

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72162-1912-2721621912021 BOTTLE in 1 CARTON (72162-1912-2) / 118 mL in 1 BOTTLE1 bottle2024-12-24NoNoHistorical