Tylenol PM - 50580-482-68 - (Acetaminophen and Diphenhydramine Hydrochloride)

Alphabetical Index


Drug Information of Tylenol PM

Product NDC: 50580-482
Proprietary Name: Tylenol PM
Non Proprietary Name: Acetaminophen and Diphenhydramine Hydrochloride
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen and Diphenhydramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tylenol PM

Product NDC: 50580-482
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19910424

Package Information of Tylenol PM

Package NDC: 50580-482-68
Package Description: 34 POUCH in 1 CARTON (50580-482-68) > 2 TABLET, FILM COATED in 1 POUCH

NDC Information of Tylenol PM

NDC Code 50580-482-68
Proprietary Name Tylenol PM
Package Description 34 POUCH in 1 CARTON (50580-482-68) > 2 TABLET, FILM COATED in 1 POUCH
Product NDC 50580-482
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Diphenhydramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19910424
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Tylenol PM


General Information