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WAL-DRYL Allergy - 0363-0329-22 - (Diphenhydramine HCl)

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Drug Information of WAL-DRYL Allergy

Product NDC: 0363-0329
Proprietary Name: WAL-DRYL Allergy
Non Proprietary Name: Diphenhydramine HCl
Active Ingredient(s): 25    mg/1 & nbsp;   Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of WAL-DRYL Allergy

Product NDC: 0363-0329
Labeler Name: WALGREEN CO.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19900302

Package Information of WAL-DRYL Allergy

Package NDC: 0363-0329-22
Package Description: 1 BLISTER PACK in 1 CARTON (0363-0329-22) > 48 TABLET in 1 BLISTER PACK

NDC Information of WAL-DRYL Allergy

NDC Code 0363-0329-22
Proprietary Name WAL-DRYL Allergy
Package Description 1 BLISTER PACK in 1 CARTON (0363-0329-22) > 48 TABLET in 1 BLISTER PACK
Product NDC 0363-0329
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900302
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name WALGREEN CO.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of WAL-DRYL Allergy


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