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Acetaminophen PM - 68391-161-05 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of Acetaminophen PM

Product NDC: 68391-161
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: 68391-161
Labeler Name: BJWC (Berkley & Jensen / BJ's)
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20130115

Package Information of Acetaminophen PM

Package NDC: 68391-161-05
Package Description: 500 TABLET, COATED in 1 BOTTLE (68391-161-05)

NDC Information of Acetaminophen PM

NDC Code 68391-161-05
Proprietary Name Acetaminophen PM
Package Description 500 TABLET, COATED in 1 BOTTLE (68391-161-05)
Product NDC 68391-161
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20130115
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name BJWC (Berkley & Jensen / BJ's)
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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