Acetaminophen

Product NDC
21130-760
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Safeway Inc.
Application
ANDA076200
Marketing category
ANDA
Substance
ACETAMINOPHEN
Current FDA listing
Historical FDA.report record

Related Records

Packages

No records found.

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
ACETAMINOPHENSafeway Inc. | Ohm Laboratories Inc.2018-06-15HUMAN OTC DRUG LABEL1
Drug FactsSafeway Inc. | Ohm Laboratories Inc.2012-09-26HUMAN OTC DRUG LABEL2