Allergy - 59779-923-08 - (Diphenhydramine HCl)

Alphabetical Index


Drug Information of Allergy

Product NDC: 59779-923
Proprietary Name: 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 Allergy

Product NDC: 59779-923
Labeler Name: WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19900302

Package Information of Allergy

Package NDC: 59779-923-08
Package Description: 1 BLISTER PACK in 1 CARTON (59779-923-08) > 24 TABLET in 1 BLISTER PACK

NDC Information of Allergy

NDC Code 59779-923-08
Proprietary Name Allergy
Package Description 1 BLISTER PACK in 1 CARTON (59779-923-08) > 24 TABLET in 1 BLISTER PACK
Product NDC 59779-923
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 WOONSOCKET PRESCRIPTION CENTER,INCORPORATED
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Allergy


General Information