NDC 50090-1638

Pharbedryl

Diphenhydramine Hcl

Pharbedryl is a Oral Capsule in the Human Otc Drug category. It is labeled and distributed by A-s Medication Solutions. The primary component is Diphenhydramine Hydrochloride.

Product ID50090-1638_10fc2a98-6c58-406f-bde3-c0fb4553a0b8
NDC50090-1638
Product TypeHuman Otc Drug
Proprietary NamePharbedryl
Generic NameDiphenhydramine Hcl
Dosage FormCapsule
Route of AdministrationORAL
Marketing Start Date2016-02-01
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart341
Labeler NameA-S Medication Solutions
Substance NameDIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength25 mg/1
Pharm ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 50090-1638-0

30 CAPSULE in 1 BOTTLE (50090-1638-0)
Marketing Start Date2016-02-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50090-1638-1 [50090163801]

Pharbedryl CAPSULE
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2015-01-15
Inactivation Date2020-01-31
Reactivation Date2020-02-14

NDC 50090-1638-8 [50090163808]

Pharbedryl CAPSULE
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2015-01-15
Inactivation Date2020-01-31
Reactivation Date2020-02-14

NDC 50090-1638-0 [50090163800]

Pharbedryl CAPSULE
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2015-01-15
Inactivation Date2020-01-31
Reactivation Date2020-02-14

NDC 50090-1638-3 [50090163803]

Pharbedryl CAPSULE
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2015-01-15
Inactivation Date2020-01-31
Reactivation Date2020-02-14

NDC 50090-1638-2 [50090163802]

Pharbedryl CAPSULE
Marketing CategoryOTC monograph final
Application Numberpart341
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2015-01-15
Inactivation Date2020-01-31
Reactivation Date2020-02-14

Drug Details

Active Ingredients

IngredientStrength
DIPHENHYDRAMINE HYDROCHLORIDE25 mg/1

OpenFDA Data

SPL SET ID:f155295c-4500-4af6-98df-a64cedda385c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1049909
  • NDC Crossover Matching brand name "Pharbedryl" or generic name "Diphenhydramine Hcl"

    NDCBrand NameGeneric Name
    16103-347PharbedrylPharbedryl
    16103-348PharbedrylPharbedryl
    50090-1639PharbedrylPharbedryl
    50090-2162PharbedrylPharbedryl
    50090-1638PharbedrylPharbedryl
    50090-1640PharbedrylPharbedryl
    67046-006PharbedrylPharbedryl
    67046-007PharbedrylPharbedryl
    73057-347PHARBEDRYLPHARBEDRYL
    70934-445PharbedrylPharbedryl
    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
    0363-0329WAL-DRYL ALLERGYDiphenhydramine HCl
    0363-0020Wal-Sleep ZDiphenhydramine HCl

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.