up and up ibuprofen

Product NDC
11673-514
11-digit product format
116730514
Labeler code
11673
Product ID
11673-514_2eb3a00e-a0e2-4a19-bbf8-9d093a8a0b50
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Target Corporation
Application
ANDA203599
Marketing category
ANDA
Marketing start
2018-12-28
Marketing end
0000-00-00
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-514UP AND UP IBUPROFEN (IBUPROFEN) CAPSULE, LIQUID FILLED [TARGET CORPORATION]5Legacy NDC20250223_3f349e32-10fe-4cc2-b3ce-235a640bc727.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-514-06116730514061 BOTTLE in 1 CARTON (11673-514-06) > 160 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2018-12-280000-00-00NoNoCurrent
11673-514-27116730514271 BOTTLE in 1 CARTON (11673-514-27) > 180 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2018-12-280000-00-00NoNoCurrent
11673-514-58116730514581 BOTTLE in 1 CARTON (11673-514-58) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2018-12-282023-07-31NoNoCurrent
11673-514-76116730514761 BOTTLE in 1 CARTON (11673-514-76) > 120 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2018-12-280000-00-00NoNoCurrent
11673-514-8711673051487300 CAPSULE, LIQUID FILLED in 1 BOTTLE (11673-514-87) 2019-04-090000-00-00NoNoCurrent