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Antihistamine Allergy - 37808-329-08 - (Diphenhydramine HCl)

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Drug Information of Antihistamine Allergy

Product NDC: 37808-329
Proprietary Name: Antihistamine Allergy
Non Proprietary Name: Diphenhydramine HCl
Active Ingredient(s): 25    mg/1 & nbsp;   Diphenhydramine HCl
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Antihistamine Allergy

Product NDC: 37808-329
Labeler Name: H E B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19900302

Package Information of Antihistamine Allergy

Package NDC: 37808-329-08
Package Description: 2 BLISTER PACK in 1 CARTON (37808-329-08) > 12 CAPSULE, COATED in 1 BLISTER PACK

NDC Information of Antihistamine Allergy

NDC Code 37808-329-08
Proprietary Name Antihistamine Allergy
Package Description 2 BLISTER PACK in 1 CARTON (37808-329-08) > 12 CAPSULE, COATED in 1 BLISTER PACK
Product NDC 37808-329
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Diphenhydramine HCl
Dosage Form Name CAPSULE, COATED
Route Name ORAL
Start Marketing Date 19900302
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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