FDA.reportPublic FDA data

Ibuprofen

Product NDC
41163-312
11-digit product format
411630312
Labeler code
41163
Product ID
41163-312_38dea47a-5c82-55e1-e063-6294a90a66e2
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
United Natural Foods, Inc. dba UNFI
Application
ANDA202312
Marketing category
ANDA
Marketing start
2020-01-01
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41163-312-02Ibuprofen1 in 1 CARTONTABLET, COATED14
41163-312-02Ibuprofen50 in 1 BOTTLE, PLASTICTABLET, COATED504
41163-312-03Ibuprofen100 in 1 BOTTLE, PLASTICTABLET, COATED1004
41163-312-03Ibuprofen1 in 1 CARTONTABLET, COATED14
41163-312-05Ibuprofen500 in 1 BOTTLE, PLASTICTABLET, COATED5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41163-312IBUPROFEN TABLET, COATED [UNITED NATURAL FOODS, INC. DBA UNFI]3Current NDC, Legacy NDC, 5 package rows20230519_8fed1f86-49a0-4747-e053-2a95a90a42b8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSN8fed1f86-49a0-4747-e053-2a95a90a42b84
310965ibuprofen 200 MG Oral TabletSCD8fed1f86-49a0-4747-e053-2a95a90a42b84
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY8fed1f86-49a0-4747-e053-2a95a90a42b84

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
41163-312-02411630312021 BOTTLE, PLASTIC in 1 CARTON (41163-312-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC2020-01-010000-00-00NoNoCurrent
41163-312-03411630312031 BOTTLE, PLASTIC in 1 CARTON (41163-312-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC2020-01-010000-00-00NoNoCurrent
41163-312-0541163031205500 TABLET, COATED in 1 BOTTLE, PLASTIC (41163-312-05) 2020-01-010000-00-00NoNoCurrent