FDA.reportPublic FDA data

NDC 70436-097

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
70436-097
Current FDA listing
Not matched in FDA.report NDC product tables

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70436-097-012026-01-29C16284748780-149896155-a347-586f-e063-e6dba90add90218201c5-e219-4dcb-ab6d-d6efe33d9f62
70436-097-042026-01-29C16284748780-149896155-a347-586f-e063-e6dba90add90218201c5-e219-4dcb-ab6d-d6efe33d9f62

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70436-097LURASIDONE HYDROCHLORIDE TABLET, FILM COATED [SLATE RUN PHARMACEUTICALS, LLC]2Unmatched20230414_218201c5-e219-4dcb-ab6d-d6efe33d9f62.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
70436-097-04EA - Each70436-097aadad105-7923-4242-a326-f04ada43508912023-03-13