KINEVAC - 0270-0556-15 - (sincalide)

Alphabetical Index


Drug Information of KINEVAC

Product NDC: 0270-0556
Proprietary Name: KINEVAC
Non Proprietary Name: sincalide
Active Ingredient(s): 5    ug/5mL & nbsp;   sincalide
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of KINEVAC

Product NDC: 0270-0556
Labeler Name: Bracco Diagnostics Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017697
Marketing Category: NDA
Start Marketing Date: 19760721

Package Information of KINEVAC

Package NDC: 0270-0556-15
Package Description: 10 VIAL in 1 PACKAGE (0270-0556-15) > 5 mL in 1 VIAL

NDC Information of KINEVAC

NDC Code 0270-0556-15
Proprietary Name KINEVAC
Package Description 10 VIAL in 1 PACKAGE (0270-0556-15) > 5 mL in 1 VIAL
Product NDC 0270-0556
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name sincalide
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19760721
Marketing Category Name NDA
Labeler Name Bracco Diagnostics Inc.
Substance Name SINCALIDE
Strength Number 5
Strength Unit ug/5mL
Pharmaceutical Classes Cholecystokinin [Chemical/Ingredient],Cholecystokinin Analog [EPC]

Complete Information of KINEVAC


General Information