Ibuprofen

Product NDC
76420-575
11-digit product format
764200575
Labeler code
76420
Product ID
76420-575_0706e837-6b65-31c5-e063-6294a90a85e5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
Asclemed USA, Inc.
Application
ANDA213794
Marketing category
ANDA
Marketing start
2020-05-08
Substance
IBUPROFEN
Active strength
400 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 formatDescriptionUnitsMarketing startSampleExclude flagStatus
76420-575-0176420057501100 TABLET in 1 BOTTLE (76420-575-01) 100 tablet2023-07-20NoNoHistorical
76420-575-307642005753030 TABLET in 1 BOTTLE (76420-575-30) 30 tablet2023-07-20NoNoHistorical
76420-575-607642005756060 TABLET in 1 BOTTLE (76420-575-60) 60 tablet2023-07-20NoNoHistorical
76420-575-907642005759090 TABLET in 1 BOTTLE (76420-575-90) 90 tablet2023-07-20NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USP Rx onlyAsclemed USA, Inc. | ASCLEMED USA INC. DBA ENOVACHEM2023-10-06HUMAN PRESCRIPTION DRUG LABEL2