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Allergy Relief - 50844-329-08 - (Diphenhydramine HCl)

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Drug Information of Allergy Relief

Product NDC: 50844-329
Proprietary Name: Allergy Relief
Non Proprietary Name: Diphenhydramine HCl
Active Ingredient(s): 25    mg/1 & nbsp;   Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Allergy Relief

Product NDC: 50844-329
Labeler Name: L.N.K. International, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19900302

Package Information of Allergy Relief

Package NDC: 50844-329-08
Package Description: 1 BLISTER PACK in 1 CARTON (50844-329-08) > 24 TABLET, COATED in 1 BLISTER PACK

NDC Information of Allergy Relief

NDC Code 50844-329-08
Proprietary Name Allergy Relief
Package Description 1 BLISTER PACK in 1 CARTON (50844-329-08) > 24 TABLET, COATED in 1 BLISTER PACK
Product NDC 50844-329
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine HCl
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19900302
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name L.N.K. International, Inc.
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Allergy Relief


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