FDA.reportPublic FDA data

NDC 0078-0881 - KISQALI FEMARA CO-PACK

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
0078-0881
Package NDCs from labels
0078-0881-50
Manufacturer
Novartis Pharmaceuticals Corporation
Effective date
2025-09-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
KISQALI FEMARA CO-PACK - Novartis Pharmaceuticals CorporationNovartis Pharmaceuticals Corporation2025-09-16HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0078-0881-50KISQALI FEMARA CO-PACK28 in 1 BOTTLE, PLASTICTABLET, FILM COATED282.5 mg25
0078-0881-50KISQALI FEMARA CO-PACK28 in 1 BOTTLE, PLASTICTABLET, FILM COATED282.5 mg25
0078-0881-50KISQALI FEMARA CO-PACK28 in 1 BOTTLE, PLASTICTABLET, FILM COATED282.5 mg25

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0078-0881KISQALI FEMARA CO-PACK (LETROZOLE AND RIBOCICLIB) KIT [NOVARTIS PHARMACEUTICALS CORPORATION]23Unmatched20250303_aa5e4446-19cd-4235-a382-5b48bf6c3b2f.zip