Acetaminophen 8 Hour

Product NDC
41163-336
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Supervalu Inc.
Application
ANDA076200
Marketing category
ANDA
Substance
ACETAMINOPHEN
Current FDA listing
Historical FDA.report record

Related Records

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Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsSupervalu Inc. | Ranbaxy Pharmaceuticals Inc. | Ohm Laboratories Inc.2013-09-05HUMAN OTC DRUG LABEL1