NDC 75907-075-28 - ERRIN

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: 75907-075
Requested NDC: 75907-075-28
Package NDCs from labels: 75907-075-28, 75907-075-32
Manufacturer: Dr. Reddy's Labratories Inc.
Effective date: 2024-03-01
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
ERRIN ® (NORETHINDRONE TABLETS USP, 0.35 MG)	Dr. Reddy's Labratories Inc.	2024-03-01	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
75907-075-28	ERRIN	28 in 1 BLISTER PACK	TABLET	28		1
75907-075-32	ERRIN	3 in 1 CARTON	TABLET	3		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
75907-075	ERRIN (NORETHINDRONE) TABLET [DR. REDDY'S LABRATORIES INC.]	1	Current NDC, 2 package rows	20240310_df29577b-c2f0-bea8-b048-7719972707aa.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
75907-075-28	EA - Each	75907-075	58636e75-a92a-4f59-adbd-08f04b5b3b4d	1	2024-06-10
75907-075-32	EA - Each	75907-075	bcaad4f1-a360-4fd0-b619-b0a5a4661037	1	2024-06-10

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 2 of 2 · 26 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Emzahh	NORETHINDRONE	Aurobindo Pharma Limited	197d31d3-eec8-49c7-9640-918ff138fea2	2023-04-10	Warnings, Adverse reactions	Exact identifier rxcui: 748961 rxcui: 198042 unii: T18F433X4S
Lyleq	NORETHINDRONE	Afaxys Pharma, LLC	c9f00a3e-c827-4066-bf85-079b3a20f25e	2023-03-27	Warnings, Adverse reactions	Exact identifier rxcui: 748961 rxcui: 198042 unii: T18F433X4S
Nortrel 28 Day	NORETHINDRONE AND ETHINYL ESTRADIOL	Teva Pharmaceuticals USA, Inc.	140c50d6-c931-423a-9aa0-526eae7ab93c	2021-12-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: T18F433X4S
Incassia	NORETHINDRONE	Aurobindo Pharma Limited	0b87cef0-610c-469d-92ba-4007f4bc3878	2021-09-14	Warnings, Adverse reactions	Exact identifier rxcui: 748961 rxcui: 198042 unii: T18F433X4S
Norethindrone	NORETHINDRONE	Proficient Rx LP	fb84b86e-5f1f-4c17-8b69-ff695c5faf55	2019-11-01	Warnings, Adverse reactions	Exact identifier rxcui: 748961 rxcui: 198042 unii: T18F433X4S
NORETHINDRONE	NORETHINDRONE	Mylan Pharmaceuticals Inc.	af851d82-b30f-463b-9dba-0437225dc1ee	2018-10-23	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 748961 rxcui: 198042 unii: T18F433X4S

Reported adverse events (FAERS/openFDA)#

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