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acetaminophen pm - 11822-0837-1 - (Acetaminophen, Diphenhydramine HCl)

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Drug Information of acetaminophen pm

Product NDC: 11822-0837
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: 11822-0837
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: part338
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20011002

Package Information of acetaminophen pm

Package NDC: 11822-0837-1
Package Description: 1 BOTTLE in 1 CARTON (11822-0837-1) > 50 TABLET, COATED in 1 BOTTLE

NDC Information of acetaminophen pm

NDC Code 11822-0837-1
Proprietary Name acetaminophen pm
Package Description 1 BOTTLE in 1 CARTON (11822-0837-1) > 50 TABLET, COATED in 1 BOTTLE
Product NDC 11822-0837
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20011002
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rite Aid Corporation
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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