NDC 43547-382

donepezil hydrochloride

Donepezil Hydrochloride

donepezil hydrochloride is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Solco Healthcare Us, Llc. The primary component is Donepezil Hydrochloride.

Product ID43547-382_0de518b0-75a0-466f-9e20-15c2e00aefbd
NDC43547-382
Product TypeHuman Prescription Drug
Proprietary Namedonepezil hydrochloride
Generic NameDonepezil Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2016-12-05
Marketing CategoryANDA / ANDA
Application NumberANDA203713
Labeler NameSolco Healthcare US, LLC
Substance NameDONEPEZIL HYDROCHLORIDE
Active Ingredient Strength23 mg/1
Pharm ClassesCholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 43547-382-03

30 TABLET, FILM COATED in 1 BOTTLE (43547-382-03)
Marketing Start Date2016-12-05
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 43547-382-10 [43547038210]

donepezil hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203713
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-05
Inactivation Date2020-01-31
Reactivation Date2020-03-05

NDC 43547-382-03 [43547038203]

donepezil hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203713
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-12-05
Inactivation Date2020-01-31
Reactivation Date2020-03-05

NDC 43547-382-09 [43547038209]

donepezil hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203713
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2016-12-05
Inactivation Date2020-01-31
Reactivation Date2020-03-05

NDC 43547-382-50 [43547038250]

donepezil hydrochloride TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA203713
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-12-05
Inactivation Date2020-01-31
Reactivation Date2020-03-05

Drug Details

Active Ingredients

IngredientStrength
DONEPEZIL HYDROCHLORIDE23 mg/1

OpenFDA Data

SPL SET ID:64c81ee1-aee6-4f44-b048-c301d0304ff5
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1100184

    • Pharmacological Class

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

    Medicade Reported Pricing

    43547038209 DONEPEZIL HCL 23 MG TABLET

    Pricing Unit: EA | Drug Type:

    43547038203 DONEPEZIL HCL 23 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.