NDC 42543-703

Donepezil Hydrochloride

Donepezil Hydrochloride

Donepezil Hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Vensun Pharmaceuticals, Inc.. The primary component is Donepezil Hydrochloride.

Product ID42543-703_a73d19f0-cd8e-4b4a-8ded-b9e028305958
NDC42543-703
Product TypeHuman Prescription Drug
Proprietary NameDonepezil Hydrochloride
Generic NameDonepezil Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2014-12-10
Marketing CategoryANDA / ANDA
Application NumberANDA203907
Labeler NameVensun Pharmaceuticals, Inc.
Substance NameDONEPEZIL HYDROCHLORIDE
Active Ingredient Strength10 mg/1
Pharm ClassesCholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 42543-703-05

500 TABLET, FILM COATED in 1 BOTTLE (42543-703-05)
Marketing Start Date2014-12-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 42543-703-01 [42543070301]

Donepezil Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203907
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-10
Inactivation Date2020-01-31

NDC 42543-703-90 [42543070390]

Donepezil Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203907
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-10
Inactivation Date2020-01-31

NDC 42543-703-05 [42543070305]

Donepezil Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203907
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-10
Inactivation Date2020-01-31

NDC 42543-703-30 [42543070330]

Donepezil Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203907
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-10
Inactivation Date2020-01-31

NDC 42543-703-10 [42543070310]

Donepezil Hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203907
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-12-10
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DONEPEZIL HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:851107e7-143c-47f3-8168-1bf197b91c1e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 997229
  • 997223
    • UPC Code
  • 0342543702301
  • 0342543703308

    • Pharmacological Class

    • Cholinesterase Inhibitor [EPC]
    • Cholinesterase Inhibitors [MoA]

    Medicade Reported Pricing

    42543070390 DONEPEZIL HCL 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    42543070330 DONEPEZIL HCL 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    42543070310 DONEPEZIL HCL 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    42543070305 DONEPEZIL HCL 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Donepezil Hydrochloride" or generic name "Donepezil Hydrochloride"

    NDCBrand NameGeneric Name
    0143-9747Donepezil HydrochlorideDonepezil Hydrochloride
    0143-9748Donepezil HydrochlorideDonepezil Hydrochloride
    0179-0208DONEPEZIL HYDROCHLORIDEDONEPEZIL HYDROCHLORIDE
    0228-4529Donepezil hydrochlorideDonepezil hydrochloride
    0378-1025Donepezil Hydrochloridedonepezil hydrochloride
    0615-7623donepezil hydrochlorideDONEPEZIL HYDROCHLORIDE
    0615-7624donepezil hydrochlorideDONEPEZIL HYDROCHLORIDE
    0615-7653Donepezil hydrochlorideDonepezil hydrochloride
    0615-7654Donepezil hydrochlorideDonepezil hydrochloride
    0615-7842Donepezil HydrochlorideDonepezil Hydrochloride
    0615-7843Donepezil HydrochlorideDonepezil Hydrochloride
    0615-7951Donepezil HydrochlorideDonepezil Hydrochloride
    0615-7952Donepezil HydrochlorideDonepezil Hydrochloride
    0615-8313Donepezil HydrochlorideDonepezil Hydrochloride
    0781-5274Donepezil HydrochlorideDonepezil Hydrochloride
    0781-5275Donepezil HydrochlorideDonepezil Hydrochloride
    0781-5276Donepezil Hydrochloridedonepezil hydrochloride
    0781-5277Donepezil Hydrochloridedonepezil hydrochloride
    0904-6408Donepezil HydrochlorideDonepezil Hydrochloride
    0904-6409Donepezil HydrochlorideDonepezil Hydrochloride
    0904-6477Donepezil HydrochlorideDonepezil Hydrochloride
    0904-6478Donepezil HydrochlorideDonepezil Hydrochloride
    13668-102Donepezil HydrochlorideDonepezil Hydrochloride
    13668-103Donepezil HydrochlorideDonepezil Hydrochloride
    16571-778Donepezil HydrochlorideDonepezil Hydrochloride
    16571-779Donepezil HydrochlorideDonepezil Hydrochloride
    68071-1572donepezil hydrochloridedonepezil hydrochloride
    68071-1523donepezil hydrochloridedonepezil hydrochloride
    68071-1700donepezil hydrochloridedonepezil hydrochloride
    68071-4008Donepezil HydrochlorideDonepezil Hydrochloride
    68071-3396donepezil hydrochloridedonepezil hydrochloride
    68151-3114Donepezil HydrochlorideDonepezil Hydrochloride
    68180-527DONEPEZIL HYDROCHLORIDEDONEPEZIL HYDROCHLORIDE
    68382-347donepezil hydrochloridedonepezil hydrochloride
    68382-521donepezil hydrochloridedonepezil hydrochloride
    68382-303donepezil hydrochloridedonepezil hydrochloride
    68382-346donepezil hydrochloridedonepezil hydrochloride
    68382-302donepezil hydrochloridedonepezil hydrochloride
    69150-415Donepezil HydrochlorideDonepezil Hydrochloride
    69150-416Donepezil HydrochlorideDonepezil Hydrochloride
    70518-0452donepezil hydrochloridedonepezil hydrochloride
    70518-0802Donepezil HydrochlorideDonepezil Hydrochloride
    70518-1445Donepezil HydrochlorideDonepezil Hydrochloride
    70518-1666donepezil hydrochloridedonepezil hydrochloride
    70771-1320donepezil hydrochloridedonepezil hydrochloride
    71209-020DONEPEZIL HYDROCHLORIDEDONEPEZIL HYDROCHLORIDE
    71335-0416Donepezil HydrochlorideDonepezil Hydrochloride
    71209-019DONEPEZIL HYDROCHLORIDEDONEPEZIL HYDROCHLORIDE
    71335-0582Donepezil HydrochlorideDonepezil Hydrochloride
    71335-0876Donepezil HydrochlorideDonepezil Hydrochloride
    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.