Ibuprofen, Caseys, 50ct

Product NDC
66715-6407
11-digit product format
667156407
Labeler code
66715
Product ID
66715-6407_1ab6fbae-ead6-283b-e063-6394a90a4ed4
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Lil' Drug Store Products, Inc.
Application
ANDA079129
Marketing category
ANDA
Marketing start
2024-04-01
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

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
WK2XYI10QMIBUPROFEN15687-27-1IBUPROFEN

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
66715-6407-4667156407041 BOTTLE, PLASTIC in 1 CARTON (66715-6407-4) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC2024-04-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
IbuprofenLil' Drug Store Products, Inc.2024-06-12HUMAN OTC DRUG LABEL1