Bicisate

Product NDC
51808-217
11-digit product format
518080217
Labeler code
51808
Product ID
51808-217_b780bd14-67f7-4dd6-8d36-f53a6d38152c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Bicisate
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Labeler
AnazaoHealth Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2012-05-23
Marketing end
0000-00-00
Substance
BICISATE
Active strength
1 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51808-217-012019-11-27C16284748780-19855d018-e156-cd31-e053-dbdaa90ab51aBicisate (ECD) (for the preparation of Tc99m Bicisate injection)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51808-217-01Bicisate1 in 1 KITINJECTION, POWDER, LYOPHILIZED,11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51808-217BICISATE INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ANAZAOHEALTH CORPORATION]1Legacy NDC, 1 package rows20121015_e094cb1d-80fe-4277-b8f4-9817918f8c76.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
51808-217-01518080217011 in 1 KITHistorical