NDC 78206-146-01 - NuvaRing

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
78206-146
Requested NDC
78206-146-01
Package NDCs from labels
78206-146-01, 78206-146-03
Manufacturer
Organon LLC
Effective date
2025-11-14
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
NuvaRing - Organon LLCOrganon LLC2025-11-14HUMAN PRESCRIPTION DRUG LABEL
NUVARING - A-S Medication SolutionsA-S Medication Solutions2024-03-10HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78206-146-01NuvaRing21 d in 1 POUCHINSERT, EXTENDED RELEASE2110
78206-146-03NuvaRing3 in 1 BOXINSERT, EXTENDED RELEASE310

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78206-146NUVARING (ETONOGESTREL AND ETHINYL ESTRADIOL) INSERT, EXTENDED RELEASE [ORGANON LLC]9Current NDC, Legacy NDC, 2 package rows20241228_55eb60e3-6f4d-40a3-8ee6-e7fd2d0c7d97.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
78206-146-01EA - Each78206-14646958e76-d223-4388-a3fe-118e924e132f12021-08-05
78206-146-03EA - Each78206-146a2f52081-a224-4228-8735-ce3efabf8f3312021-08-05

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 3 · 41 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Nortrel 28 DayNORETHINDRONE AND ETHINYL ESTRADIOLTeva Pharmaceuticals USA, Inc.140c50d6-c931-423a-9aa0-526eae7ab93c2021-12-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 423D2T571U

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.