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pain relief pm - 56062-751-78 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of pain relief pm

Product NDC: 56062-751
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of pain relief pm

Product NDC: 56062-751
Labeler Name: Publix Super Markets Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120130

Package Information of pain relief pm

Package NDC: 56062-751-78
Package Description: 1 BOTTLE in 1 CARTON (56062-751-78) > 100 TABLET, FILM COATED in 1 BOTTLE

NDC Information of pain relief pm

NDC Code 56062-751-78
Proprietary Name pain relief pm
Package Description 1 BOTTLE in 1 CARTON (56062-751-78) > 100 TABLET, FILM COATED in 1 BOTTLE
Product NDC 56062-751
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120130
Marketing Category Name OTC MONOGRAPH NOT 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


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