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good sense pain relief pm - 0113-0751-71 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of good sense pain relief pm

Product NDC: 0113-0751
Proprietary Name: good sense 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 good sense pain relief pm

Product NDC: 0113-0751
Labeler Name: L Perrigo Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20120125

Package Information of good sense pain relief pm

Package NDC: 0113-0751-71
Package Description: 1 BOTTLE in 1 CARTON (0113-0751-71) > 50 TABLET, FILM COATED in 1 BOTTLE

NDC Information of good sense pain relief pm

NDC Code 0113-0751-71
Proprietary Name good sense pain relief pm
Package Description 1 BOTTLE in 1 CARTON (0113-0751-71) > 50 TABLET, FILM COATED in 1 BOTTLE
Product NDC 0113-0751
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120125
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name L Perrigo Company
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of good sense pain relief pm


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