Tylenol PM - 50580-244-03 - (Acetaminophen and Diphenhydramine hydrochloride)

Alphabetical Index


Drug Information of Tylenol PM

Product NDC: 50580-244
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Tylenol PM

Product NDC: 50580-244
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: 20070801

Package Information of Tylenol PM

Package NDC: 50580-244-03
Package Description: 2 TABLET, COATED in 1 POUCH (50580-244-03)

NDC Information of Tylenol PM

NDC Code 50580-244-03
Proprietary Name Tylenol PM
Package Description 2 TABLET, COATED in 1 POUCH (50580-244-03)
Product NDC 50580-244
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Diphenhydramine hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20070801
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