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Wal-Nadol PM - 0363-0235-29 - (Acetaminophen and Diphenhydramine HCl)

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Drug Information of Wal-Nadol PM

Product NDC: 0363-0235
Proprietary Name: Wal-Nadol PM
Non Proprietary Name: Acetaminophen and Diphenhydramine HCl
Active Ingredient(s): 500; 25    mg/1; mg/1 & nbsp;   Acetaminophen and Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Wal-Nadol PM

Product NDC: 0363-0235
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19940515

Package Information of Wal-Nadol PM

Package NDC: 0363-0235-29
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0363-0235-29) > 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Wal-Nadol PM

NDC Code 0363-0235-29
Proprietary Name Wal-Nadol PM
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0363-0235-29) > 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 0363-0235
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen and Diphenhydramine HCl
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19940515
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name WALGREEN CO.
Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 500; 25
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Wal-Nadol PM


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