Ibuprofen

Product NDC
66267-115
11-digit product format
662670115
Labeler code
66267
Product ID
66267-115_1bbdab14-0ce5-b300-e063-6394a90a5175
Type
HUMAN OTC DRUG
Nonproprietary name
ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA075010
Marketing category
ANDA
Marketing start
2004-01-01
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
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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66267-115-20Ibuprofen20 in 1 BOTTLETABLET, FILM COATED205
66267-115-30Ibuprofen30 in 1 BOTTLETABLET, FILM COATED305
66267-115-50Ibuprofen50 in 1 BOTTLETABLET, FILM COATED505

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-115-20EA - Each66267-1151c3ba37d-74a9-4e62-b8d4-2df569d0185712016-11-08
66267-115-30EA - Each66267-115cb22a687-1744-469b-9985-ca9fec2a019d12016-11-08
66267-115-50EA - Each66267-1156708a40d-a563-48c9-8cb4-023b6ab95ace12016-11-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66267-115IBUPROFEN TABLET, FILM COATED [NUCARE PHARMACEUTICALS, INC.]5Current NDC, Legacy NDC, 3 package rows20240627_3e3848f2-4922-39ea-e054-00144ff88e88.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSN3e3848f2-4922-39ea-e054-00144ff88e885
310965ibuprofen 200 MG Oral TabletSCD3e3848f2-4922-39ea-e054-00144ff88e885
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY3e3848f2-4922-39ea-e054-00144ff88e885

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
66267-115-206626701152020 TABLET, FILM COATED in 1 BOTTLE (66267-115-20) 2016-10-060000-00-00NoNoCurrent
66267-115-306626701153030 TABLET, FILM COATED in 1 BOTTLE (66267-115-30) 2016-10-060000-00-00NoNoCurrent
66267-115-506626701155050 TABLET, FILM COATED in 1 BOTTLE (66267-115-50) 2016-10-060000-00-00NoNoCurrent