NDC 47781-147

Gadopentetate dimeglumine

Gadopentetate Dimeglumine

Gadopentetate dimeglumine is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Alvogen, Inc. The primary component is Gadopentetate Dimeglumine.

Product ID47781-147_1d137c2c-fd59-4203-8115-b0a25a282bef
NDC47781-147
Product TypeHuman Prescription Drug
Proprietary NameGadopentetate dimeglumine
Generic NameGadopentetate Dimeglumine
Dosage FormInjection
Route of AdministrationINTRAVENOUS
Marketing Start Date2014-02-24
Marketing CategoryNDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC
Application NumberNDA019596
Labeler NameAlvogen, Inc
Substance NameGADOPENTETATE DIMEGLUMINE
Active Ingredient Strength469 mg/mL
NDC Exclude FlagE
Listing Certified Through2018-12-31

Packaging

NDC 47781-147-20

20 CARTON in 1 BOX (47781-147-20) > 1 VIAL, SINGLE-DOSE in 1 CARTON > 5 mL in 1 VIAL, SINGLE-DOSE
Marketing Start Date2014-02-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 47781-147-22 [47781014722]

Gadopentetate dimeglumine INJECTION
Marketing CategoryNDA authorized generic
Application NumberNDA019596
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-24
Marketing End Date2020-01-16

NDC 47781-147-29 [47781014729]

Gadopentetate dimeglumine INJECTION
Marketing CategoryNDA authorized generic
Application NumberNDA019596
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-24
Marketing End Date2020-01-16

NDC 47781-147-20 [47781014720]

Gadopentetate dimeglumine INJECTION
Marketing CategoryNDA authorized generic
Application NumberNDA019596
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-24
Marketing End Date2020-01-16

NDC 47781-147-23 [47781014723]

Gadopentetate dimeglumine INJECTION
Marketing CategoryNDA authorized generic
Application NumberNDA021037
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-24
Marketing End Date2020-01-16

NDC 47781-147-27 [47781014727]

Gadopentetate dimeglumine INJECTION
Marketing CategoryNDA authorized generic
Application NumberNDA019596
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-24
Marketing End Date2020-01-16

NDC 47781-147-25 [47781014725]

Gadopentetate dimeglumine INJECTION
Marketing CategoryNDA authorized generic
Application NumberNDA021037
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-02-24
Marketing End Date2020-01-16

Drug Details

Active Ingredients

IngredientStrength
GADOPENTETATE DIMEGLUMINE469.01 mg/mL

OpenFDA Data

SPL SET ID:25c782d4-7b45-4437-b80c-54271e3831b9
Manufacturer
UNII

NDC Crossover Matching brand name "Gadopentetate dimeglumine" or generic name "Gadopentetate Dimeglumine"

NDCBrand NameGeneric Name
47781-147Gadopentetate dimeglumineGadopentetate dimeglumine
50419-188Magnevistgadopentetate dimeglumine

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