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antihistamine allergy - 37808-462-62 - (diphenhydramine hydrochloride)

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Drug Information of antihistamine allergy

Product NDC: 37808-462
Proprietary Name: antihistamine allergy
Non Proprietary Name: diphenhydramine hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   diphenhydramine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of antihistamine allergy

Product NDC: 37808-462
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19890715

Package Information of antihistamine allergy

Package NDC: 37808-462-62
Package Description: 2 BLISTER PACK in 1 CARTON (37808-462-62) > 12 CAPSULE in 1 BLISTER PACK

NDC Information of antihistamine allergy

NDC Code 37808-462-62
Proprietary Name antihistamine allergy
Package Description 2 BLISTER PACK in 1 CARTON (37808-462-62) > 12 CAPSULE in 1 BLISTER PACK
Product NDC 37808-462
Product Type Name HUMAN OTC DRUG
Non Proprietary Name diphenhydramine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19890715
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H E B
Substance Name DIPHENHYDRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of antihistamine allergy


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