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Allergy Relief - 49348-983-04 - (Diphenhydramine HCl)

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Drug Information of Allergy Relief

Product NDC: 49348-983
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
Coding System: National Drug Codes(NDC)

Labeler Information of Allergy Relief

Product NDC: 49348-983
Labeler Name: Mckesson (Sunmark)
Product Type: HUMAN OTC DRUG
FDA Application Number: part336
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110928

Package Information of Allergy Relief

Package NDC: 49348-983-04
Package Description: 2 BLISTER PACK in 1 CARTON (49348-983-04) > 12 TABLET in 1 BLISTER PACK

NDC Information of Allergy Relief

NDC Code 49348-983-04
Proprietary Name Allergy Relief
Package Description 2 BLISTER PACK in 1 CARTON (49348-983-04) > 12 TABLET in 1 BLISTER PACK
Product NDC 49348-983
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110928
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Mckesson (Sunmark)
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Allergy Relief


General Information