NDC 51808-208

Sestamibi

Sestamibi

Sestamibi is a Intravenous Injection, Powder, Lyophilized, For Solution in the Human Prescription Drug category. It is labeled and distributed by Anazaohealth Corporation. The primary component is Tetrakis(2-methoxyisobutylisocyanide)copper(i) Tetrafluoroborate.

Product ID51808-208_118e6927-25b5-4bcc-8716-fcb5dbdc487b
NDC51808-208
Product TypeHuman Prescription Drug
Proprietary NameSestamibi
Generic NameSestamibi
Dosage FormInjection, Powder, Lyophilized, For Solution
Route of AdministrationINTRAVENOUS
Marketing Start Date2012-05-23
Marketing CategoryUNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
Labeler NameAnazaoHealth Corporation
Substance NameTETRAKIS(2-METHOXYISOBUTYLISOCYANIDE)COPPER(I) TETRAFLUOROBORATE
Active Ingredient Strength2 mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 51808-208-01

1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 KIT (51808-208-01)
Marketing Start Date2012-05-23
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51808-208-01 [51808020801]

Sestamibi INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Marketing CategoryUnapproved drug other
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-05-23
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
TETRAKIS(2-METHOXYISOBUTYLISOCYANIDE)COPPER(I) TETRAFLUOROBORATE1.5 mg/1

OpenFDA Data

SPL SET ID:5ef52f7c-042e-4f84-8048-5249bd01fade
Manufacturer
UNII

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