NDC 79929-103 - Norethindrone and ethinyl estradiol and ferrous fumarate

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
79929-103
Manufacturer
Naari Pte Limited | Naari Pharma Private Limited
Effective date
2024-04-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
norethindrone and ethinyl estradiol and ferrous fumarate tabletNaari Pte Limited | Naari Pharma Private Limited2024-04-22HUMAN PRESCRIPTION DRUG LABEL

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 11 of 11 · 202 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
NorethindroneNORETHINDRONEProficient Rx LPfb84b86e-5f1f-4c17-8b69-ff695c5faf552019-11-01Warnings, Adverse reactionsExact identifier
unii: T18F433X4S
NORETHINDRONENORETHINDRONEMylan Pharmaceuticals Inc.af851d82-b30f-463b-9dba-0437225dc1ee2018-10-23Boxed warning, Warnings, Adverse reactionsExact identifier
unii: T18F433X4S

Reported adverse events (FAERS/openFDA)#

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