ibuprofen

Product NDC
51293-844
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
ECI PHARMACEUTICALS LLC
Application
ANDA202413
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
51293-844-01100 TABLET, FILM COATED in 1 BOTTLE (51293-844-01) 2016-11-230000-00-00NoCurrent
51293-844-05500 TABLET, FILM COATED in 1 BOTTLE (51293-844-05) 2016-11-230000-00-00NoCurrent