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acetaminophen pm - 55312-829-49 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of acetaminophen pm

Product NDC: 55312-829
Proprietary Name: acetaminophen 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): CAPSULE, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of acetaminophen pm

Product NDC: 55312-829
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100826

Package Information of acetaminophen pm

Package NDC: 55312-829-49
Package Description: 1 BOTTLE in 1 CARTON (55312-829-49) > 40 CAPSULE, COATED in 1 BOTTLE

NDC Information of acetaminophen pm

NDC Code 55312-829-49
Proprietary Name acetaminophen pm
Package Description 1 BOTTLE in 1 CARTON (55312-829-49) > 40 CAPSULE, COATED in 1 BOTTLE
Product NDC 55312-829
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name CAPSULE, COATED
Route Name ORAL
Start Marketing Date 20100826
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Western Family Foods Inc
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of acetaminophen pm


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