Acetaminophen

Product NDC
15127-332
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Select Brand
Application
ANDA076200
Marketing category
ANDA
Substance
ACETAMINOPHEN
Current FDA listing
Historical FDA.report record

Related Records

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Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
80310ab1-f10f-4881-b31a-fa156db8e474Drug FactsSelect Brand | Ranbaxy Pharmaceuticals Inc. | Ohm Laboratories Inc.2012-10-02HUMAN OTC DRUG LABEL1