Home > National Drug Code (NDC) > pain relief pm

pain relief pm - 56062-837-71 - (Acetaminophen, Diphenhydramine HCl)

Alphabetical Index


Drug Information of pain relief pm

Product NDC: 56062-837
Proprietary Name: pain relief pm
Non Proprietary Name: Acetaminophen, Diphenhydramine HCl
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen, Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of pain relief pm

Product NDC: 56062-837
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20080710

Package Information of pain relief pm

Package NDC: 56062-837-71
Package Description: 1 BOTTLE in 1 CARTON (56062-837-71) > 50 TABLET, COATED in 1 BOTTLE

NDC Information of pain relief pm

NDC Code 56062-837-71
Proprietary Name pain relief pm
Package Description 1 BOTTLE in 1 CARTON (56062-837-71) > 50 TABLET, COATED in 1 BOTTLE
Product NDC 56062-837
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20080710
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Publix Super Markets Inc
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of pain relief pm


General Information