SIncalide

Product NDC
51808-203
11-digit product format
518080203
Labeler code
51808
Product ID
51808-203_8f9023fb-e982-440a-a9ee-374c4bf3153b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sincalide
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Labeler
AnazaoHealth Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2012-06-19
Marketing end
0000-00-00
Substance
SINCALIDE
Active strength
3 ug/1
Pharmacologic classes
Cholecystokinin [CS],Cholecystokinin Analog [EPC]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
957ff0e8-12af-4796-85ed-d1e36ea7fdc0Product name120230912

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51808-203-012019-11-13C16284748780-197449f38-d013-f6ea-e053-dbdaa90aa703Sincalide

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51808-203-01SIncalide1 in 1 PACKAGEINJECTION, POWDER, LYOPHILIZED,11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51808-203SINCALIDE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ANAZAOHEALTH CORPORATION]1Legacy NDC, 1 package rows20120702_c56a824b-a8ba-42db-b05c-49c731130879.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
51808-203-01518080203011 in 1 PACKAGEHistorical