Ibuprofen

Product NDC
68071-4845
11-digit product format
680714845
Labeler code
68071
Product ID
68071-4845_43cd55af-673e-5ea3-e063-6394a90a85d4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals,Inc.
Application
ANDA078329
Marketing category
ANDA
Marketing start
2014-04-01
Substance
IBUPROFEN
Active strength
800 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
IBUPROFEN800 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWK2XYI10QM
Rxcui197807

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
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
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
68071-4845-1Ibuprofen21 in 1 BOTTLETABLET, FILM COATED217
68071-4845-2Ibuprofen20 in 1 BOTTLETABLET, FILM COATED207
68071-4845-3Ibuprofen30 in 1 BOTTLETABLET, FILM COATED307

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68071-4845-3EA - Each68071-48457aed7fbd-1686-41f5-89f9-96d84d9c7b0412025-02-10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68071-4845IBUPROFEN TABLET, FILM COATED [NUCARE PHARMACEUTICALS,INC.]5Current NDC, Legacy NDC, 3 package rows20250215_86577bf3-51c6-88e2-e053-2991aa0ac741.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197807ibuprofen 800 MG Oral TabletPSN86577bf3-51c6-88e2-e053-2991aa0ac7417
197807ibuprofen 800 MG Oral TabletSCD86577bf3-51c6-88e2-e053-2991aa0ac7417

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68071-4845-16807148450121 TABLET, FILM COATED in 1 BOTTLE (68071-4845-1) 2025-02-13NoNoCurrent
68071-4845-26807148450220 TABLET, FILM COATED in 1 BOTTLE (68071-4845-2) 2019-04-120000-00-00NoNoCurrent
68071-4845-36807148450330 TABLET, FILM COATED in 1 BOTTLE (68071-4845-3) 2025-01-16NoNoCurrent