Extra Strength Pain Relief

Product NDC
82501-1575
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, COATED
Route
ORAL
Labeler
Gobrands, Inc
Application
part343
Marketing category
OTC MONOGRAPH NOT FINAL
Substance
ACETAMINOPHEN
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
82501-1575-1100 TABLET, COATED in 1 BOTTLE (82501-1575-1) 2022-05-11NoCurrent

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
0ec56ff0-e848-422c-96ec-03d1d95fdf0aExtra Strength Pain ReliefGobrands, Inc | Prodose, Inc.2024-12-20HUMAN OTC DRUG LABEL5