NDC 42507-282

Dayhist allergy

Clemastine Fumarate

Dayhist allergy is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Hyvee Inc. The primary component is Clemastine Fumarate.

Product ID42507-282_d0daae1c-f6fb-4a23-9aa9-0f68b1aea3c7
NDC42507-282
Product TypeHuman Otc Drug
Proprietary NameDayhist allergy
Generic NameClemastine Fumarate
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1996-06-21
Marketing CategoryANDA / ANDA
Application NumberANDA074512
Labeler NameHyVee Inc
Substance NameCLEMASTINE FUMARATE
Active Ingredient Strength1 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 42507-282-51

1 BLISTER PACK in 1 CARTON (42507-282-51) > 8 TABLET in 1 BLISTER PACK
Marketing Start Date1996-06-21
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 42507-282-51 [42507028251]

Dayhist allergy TABLET
Marketing CategoryANDA
Application NumberANDA074512
Product TypeHUMAN OTC DRUG
Marketing Start Date1996-06-21
Marketing End Date2020-01-28

Drug Details

Active Ingredients

IngredientStrength
CLEMASTINE FUMARATE1.34 mg/1

OpenFDA Data

SPL SET ID:d0daae1c-f6fb-4a23-9aa9-0f68b1aea3c7
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1095725
  • 857416
  • UPC Code
  • 0075450294828
  • NDC Crossover Matching brand name "Dayhist allergy" or generic name "Clemastine Fumarate"

    NDCBrand NameGeneric Name
    42507-282Dayhist allergyClemastine fumarate
    0093-0308Clemastine FumarateClemastine Fumarate
    51655-425Clemastine FumarateClemastine Fumarate
    54838-514Clemastine FumarateClemastine Fumarate
    68151-2456Clemastine FumarateClemastine Fumarate
    73308-358Clemastine FumarateClemastine Fumarate
    24385-183Good Neighbor Pharmacy Dayhist AllergyClemastine fumarate
    70000-0216Leader AllerhistClemastine fumarate
    49348-686SUNMARK 12 HOUR ALLERGY RELIEFClemastine fumarate
    0363-0707wal histClemastine fumarate

    © 2022 FDA.report
    This site is not affiliated with or endorsed by the FDA.