NDC 75907-215 - SRONYX

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: 75907-215
Manufacturer: Dr. Reddy's Labratories Inc.
Effective date: 2024-09-20
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
SRONYX ® (Levonorgestrel and Ethinyl Estradiol Tablets USP)	Dr. Reddy's Labratories Inc.	2024-09-20	HUMAN 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 9 of 9 · 161 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
My Way	LEVONORGESTREL	Lupin Pharmaceuticals,Inc.	ec01077e-ac3c-424a-9edc-0854fe0a2e0d	2016-06-17	Warnings	Exact identifier unii: 5W7SIA7YZW

Reported adverse events (FAERS/openFDA)#

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