Acetaminophen

Product NDC
46122-062
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Amerisource Bergen
Application
ANDA076200
Marketing category
ANDA
Substance
ACETAMINOPHEN
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
46122-062-7150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-062-71) 2002-04-300000-00-00NoCurrent
46122-062-78100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (46122-062-78) 2002-04-300000-00-00NoCurrent