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Acetaminophen PM - 68196-213-30 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Acetaminophen PM

Product NDC: 68196-213
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): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Acetaminophen PM

Product NDC: 68196-213
Labeler Name: SIMPLY RIGHT (Sam's West, Inc.)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130430

Package Information of Acetaminophen PM

Package NDC: 68196-213-30
Package Description: 500 TABLET, COATED in 1 BOTTLE, PLASTIC (68196-213-30)

NDC Information of Acetaminophen PM

NDC Code 68196-213-30
Proprietary Name Acetaminophen PM
Package Description 500 TABLET, COATED in 1 BOTTLE, PLASTIC (68196-213-30)
Product NDC 68196-213
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20130430
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name SIMPLY RIGHT (Sam's West, 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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