NDC 71335-0282

Digoxin

Digoxin

Digoxin is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Digoxin.

Product ID71335-0282_7fecc5ac-fa18-4aad-a3f9-89e58e0b997e
NDC71335-0282
Product TypeHuman Prescription Drug
Proprietary NameDigoxin
Generic NameDigoxin
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2002-07-26
Marketing CategoryANDA / ANDA
Application NumberANDA076268
Labeler NameBryant Ranch Prepack
Substance NameDIGOXIN
Active Ingredient Strength125 ug/1
Pharm ClassesCardiac Glycoside [EPC],Cardiac Glycosides [CS]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71335-0282-5

60 TABLET in 1 BOTTLE (71335-0282-5)
Marketing Start Date2010-03-02
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0282-4 [71335028204]

Digoxin TABLET
Marketing CategoryANDA
Application NumberANDA076268
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-02
Inactivation Date2020-01-31

NDC 71335-0282-5 [71335028205]

Digoxin TABLET
Marketing CategoryANDA
Application NumberANDA076268
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-02
Inactivation Date2020-01-31

NDC 71335-0282-1 [71335028201]

Digoxin TABLET
Marketing CategoryANDA
Application NumberANDA076268
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-02
Inactivation Date2020-01-31

NDC 71335-0282-6 [71335028206]

Digoxin TABLET
Marketing CategoryANDA
Application NumberANDA076268
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-02
Inactivation Date2020-01-31

NDC 71335-0282-3 [71335028203]

Digoxin TABLET
Marketing CategoryANDA
Application NumberANDA076268
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-02
Inactivation Date2020-01-31

NDC 71335-0282-2 [71335028202]

Digoxin TABLET
Marketing CategoryANDA
Application NumberANDA076268
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-03-02
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
DIGOXIN125 ug/1

OpenFDA Data

SPL SET ID:4b74e214-d971-41f2-9a31-ffacf0a2c031
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 197606
  • 197604
  • Pharmacological Class

    • Cardiac Glycoside [EPC]
    • Cardiac Glycosides [CS]

    NDC Crossover Matching brand name "Digoxin" or generic name "Digoxin"

    NDCBrand NameGeneric Name
    0054-0057DigoxinDigoxin
    0115-9811DigoxinDIGOXIN
    0115-9822DigoxinDIGOXIN
    0143-1240DigoxinDigoxin
    0143-1241DigoxinDigoxin
    0404-9850DigoxinDigoxin
    0615-0518DigoxinDigoxin
    0615-0547DigoxinDigoxin
    0615-7729DigoxinDigoxin
    0615-7730DigoxinDigoxin
    0615-7935DIGOXINDIGOXIN
    0615-8202DigoxinDigoxin
    0641-1410DigoxinDigoxin
    0641-6184DigoxinDigoxin
    0781-3059DigoxinDigoxin
    0904-5921DigoxinDigoxin
    68071-3011DIGOXINDIGOXIN
    68071-4398DigoxinDigoxin
    68071-4188DigoxinDigoxin
    68071-4469DigoxinDigoxin
    68094-751DigoxinDigoxin
    68084-366DigoxinDigoxin
    68084-680DigoxinDigoxin
    68094-752DigoxinDigoxin
    69238-1991DigoxinDigoxin
    69238-1992DigoxinDigoxin
    70518-0338DIGOXINDIGOXIN
    70518-0298DIGOXINDIGOXIN
    70518-0848DIGOXINDIGOXIN
    70518-1036DigoxinDigoxin
    70518-0913DIGOXINDIGOXIN
    70518-1250DigoxinDigoxin
    71335-0159DigoxinDigoxin
    71335-0282DigoxinDigoxin
    71335-1052DigoxinDigoxin
    0904-5922DigoxinDigoxin
    0904-6886DigoxinDigoxin
    16714-591DigoxinDigoxin
    17856-0057DigoxinDigoxin
    16714-590DigoxinDigoxin
    49884-514DIGOXINDIGOXIN
    49884-494DIGOXINDIGOXIN
    50090-0432DigoxinDigoxin
    50436-0324DigoxinDigoxin
    50564-544DigoxinDigoxin
    50564-545DigoxinDigoxin
    51407-125DigoxinDigoxin
    51655-000DigoxinDigoxin
    51407-126DigoxinDigoxin
    51655-001DigoxinDigoxin

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