Assured Ibuprofen

Product NDC
68210-4139
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Spirit Pharmaceuticals LLC
Application
ANDA202312
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
68210-4139-41 BOTTLE in 1 CARTON (68210-4139-4) / 40 TABLET, FILM COATED in 1 BOTTLE20210428NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
119263b5-c3b7-46dc-a3bd-9893bfd24628Ibuprofen Tablets USP 200 mgSpirit Pharmaceuticals LLC2024-12-10HUMAN OTC DRUG LABEL6