FDA.reportPublic FDA data

NDC 68180-841 - Kurvelo

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
68180-841
Package NDCs from labels
68180-841-74
Manufacturer
Lupin Pharmaceuticals, Inc. | LUPIN LIMITED
Effective date
2026-05-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Kurvelo - Lupin Pharmaceuticals, Inc. | LUPIN LIMITEDLupin Pharmaceuticals, Inc. | LUPIN LIMITED2026-05-20HUMAN PRESCRIPTION DRUG LABEL
Kurvelo - A-S Medication SolutionsA-S Medication Solutions2023-02-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68180-841-74Kurvelo21 in 1 BLISTER PACKTABLET210.15 mg12
68180-841-74Kurvelo21 in 1 BLISTER PACKTABLET210.15 mg1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68180-841KURVELO (LEVONORGESTREL AND ETHINYL ESTRADIOL) KIT [LUPIN PHARMACEUTICALS, INC.]9Unmatched20241228_752f525e-1838-4058-9ab7-2c2d91f86dfd.zip
68180-841KURVELO (LEVONORGESTREL AND ETHINYL ESTRADIOL) KIT [A-S MEDICATION SOLUTIONS]1Unmatched20230427_51e4270a-1b91-4ff8-9a50-ffe49204b6b4.zip