NDC 0363-0329

WAL-DRYL ALLERGY

Diphenhydramine Hcl

WAL-DRYL ALLERGY is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Walgreen Company. The primary component is Diphenhydramine Hydrochloride.

Product ID0363-0329_226f603a-cbd6-4c73-8efb-8a3e4e590b35
NDC0363-0329
Product TypeHuman Otc Drug
Proprietary NameWAL-DRYL ALLERGY
Generic NameDiphenhydramine Hcl
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date1990-03-02
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart341
Labeler NameWalgreen Company
Substance NameDIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength25 mg/1
NDC Exclude FlagN
Listing Certified Through2022-12-31

Packaging

NDC 0363-0329-08

2 BLISTER PACK in 1 CARTON (0363-0329-08) > 12 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date1990-03-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0363-0329-08 [00363032908]

WAL-DRYL ALLERGY TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1990-03-02

NDC 0363-0329-12 [00363032912]

WAL-DRYL ALLERGY TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1990-03-02

NDC 0363-0329-78 [00363032978]

WAL-DRYL ALLERGY TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1990-03-02

NDC 0363-0329-51 [00363032951]

WAL-DRYL ALLERGY TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-03-02

NDC 0363-0329-01 [00363032901]

WAL-DRYL ALLERGY TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Marketing Start Date1990-03-02
Marketing End Date2016-02-09

NDC 0363-0329-22 [00363032922]

WAL-DRYL ALLERGY TABLET, FILM COATED
Marketing CategoryOTC MONOGRAPH FINAL
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1990-03-02

Drug Details

Active Ingredients

IngredientStrength
DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1

OpenFDA Data

SPL SET ID:d7c2b151-f01c-4a06-b0ad-0d940de4122f
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049630
  • 1090078
  • UPC Code
  • 0311917188010
  • NDC Crossover Matching brand name "WAL-DRYL ALLERGY" or generic name "Diphenhydramine Hcl"

    NDCBrand NameGeneric Name
    0363-0329WAL-DRYL ALLERGYDiphenhydramine HCl
    0363-9685Wal-Dryl AllergyWal-Dryl Allergy
    0113-7379basic care childrens allergy reliefDiphenhydramine HCl
    0113-7186basic care nighttime sleep aidDiphenhydramine HCl
    0113-7506basic care nighttime sleep aiddiphenhydramine hcl
    0363-0481Childrens Allergy Dye-Free Wal DrylDiphenhydramine HCl
    0113-0379good sense allergyDiphenhydramine HCl
    0113-0052good sense sleep timeDiphenhydramine HCl
    0113-0186Good Sense Sleep TimeDiphenhydramine HCl
    0363-0353Itch Relief GelDiphenhydramine HCl
    0363-0236Nighttime Sleep AidDiphenhydramine HCl
    0363-0367Sleep AidDiphenhydramine HCl
    0363-0189Sleep IIDiphenhydramine HCl
    0363-0190Wal-DrylDiphenhydramine HCl
    0363-0418Wal-DrylDiphenhydramine HCl
    0363-0020Wal-Sleep ZDiphenhydramine HCl

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