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Dayhist allergy - 42507-282-51 - (Clemastine fumarate)

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Drug Information of Dayhist allergy

Product NDC: 42507-282
Proprietary Name: Dayhist allergy
Non Proprietary Name: Clemastine fumarate
Active Ingredient(s): 1.34    mg/1 & nbsp;   Clemastine fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dayhist allergy

Product NDC: 42507-282
Labeler Name: HyVee Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074512
Marketing Category: ANDA
Start Marketing Date: 19960621

Package Information of Dayhist allergy

Package NDC: 42507-282-51
Package Description: 1 BLISTER PACK in 1 CARTON (42507-282-51) > 8 TABLET in 1 BLISTER PACK

NDC Information of Dayhist allergy

NDC Code 42507-282-51
Proprietary Name Dayhist allergy
Package Description 1 BLISTER PACK in 1 CARTON (42507-282-51) > 8 TABLET in 1 BLISTER PACK
Product NDC 42507-282
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Clemastine fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960621
Marketing Category Name ANDA
Labeler Name HyVee Inc
Substance Name CLEMASTINE FUMARATE
Strength Number 1.34
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Dayhist allergy


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