Tylenol PM - 50580-176-10 - (Acetaminophen and Diphenhydramine Hydrochloride)

Alphabetical Index


Drug Information of Tylenol PM

Product NDC: 50580-176
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: 50580-176
Labeler Name: McNeil Consumer Healthcare Div. McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19911201

Package Information of Tylenol PM

Package NDC: 50580-176-10
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50580-176-10) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Information of Tylenol PM

NDC Code 50580-176-10
Proprietary Name Tylenol PM
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50580-176-10) > 100 TABLET, COATED in 1 BOTTLE, PLASTIC
Product NDC 50580-176
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Diphenhydramine Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19911201
Marketing Category Name OTC MONOGRAPH 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