SIncalide - 51808-203-01 - (Sincalide)

Alphabetical Index


Drug Information of SIncalide

Product NDC: 51808-203
Proprietary Name: SIncalide
Non Proprietary Name: Sincalide
Active Ingredient(s): 3    ug/1 & nbsp;   Sincalide
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of SIncalide

Product NDC: 51808-203
Labeler Name: AnazaoHealth Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120619

Package Information of SIncalide

Package NDC: 51808-203-01
Package Description: 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 PACKAGE (51808-203-01)

NDC Information of SIncalide

NDC Code 51808-203-01
Proprietary Name SIncalide
Package Description 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 PACKAGE (51808-203-01)
Product NDC 51808-203
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sincalide
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20120619
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name AnazaoHealth Corporation
Substance Name SINCALIDE
Strength Number 3
Strength Unit ug/1
Pharmaceutical Classes Cholecystokinin [Chemical/Ingredient],Cholecystokinin Analog [EPC]

Complete Information of SIncalide


General Information