NDC 67857-702-01 - Ismo

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: 67857-702
Requested NDC: 67857-702-01
Package NDCs from labels: 67857-702-01
Manufacturer: Reddy Pharmaceuticals, LLC
Effective date: 2007-03-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Ismo - Reddy Pharmaceuticals, LLC	Reddy Pharmaceuticals, LLC	2007-03-31	Human prescription drug label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
67857-702-01	Ismo	100 in 1 BOTTLE, PLASTIC	TABLET, FILM COATED	100		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
67857-702	ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1	1 package rows	20070426_EC09AB1C-52FA-4F41-BF65-A632DCE8F097.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
isosorbide mononitrate	ACTIVE INGREDIENT	LX1OH63030	ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
isosorbide mononitrate	ACTIVE MOIETY	LX1OH63030	ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
colloidal silicon dioxide	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
D&C Yellow 10 Aluminum Lake	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
FD&C Yellow 6 Aluminum Lake	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
hydroxypropyl cellulose	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
hydroxypropyl methylcellulose	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
lactose	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
magnesium stearate	INACTIVE INGREDIENT	70097M6I30	ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
microcrystalline cellulose	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
polyethylene glycol	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
polysorbate 20	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
povidone	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
sodium starch glycolate	INACTIVE INGREDIENT		ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1
titanium dioxide	INACTIVE INGREDIENT	15FIX9V2JP	ISMO (ISOSORBIDE MONONITRATE) TABLET, FILM COATED [REDDY PHARMACEUTICALS, LLC]	1

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 1 of 1 · 8 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Isosorbide Mononitrate	ISOSORBIDE MONONITRATE	Genus Lifesciences Inc.	0d739bf3-0672-4504-9064-b39d6b200b47	2026-04-09	Warnings, Adverse reactions	Exact identifier rxcui: 311197
Isosorbide Mononitrate	ISOSORBIDE MONONITRATE	ANI Pharmaceuticals, Inc.	06839534-85b8-42aa-b0e3-079ed236be44	2026-03-27	Warnings, Adverse reactions	Exact identifier rxcui: 311197
isosorbide mononitrate	ISOSORBIDE MONONITRATE	Coupler LLC	3e0e013f-6887-fa72-e063-6294a90a18ca	2025-09-05	Warnings, Adverse reactions	Exact identifier rxcui: 311197
isosorbide mononitrate	ISOSORBIDE MONONITRATE	OMNIVIUM PHARMACEUTICALS LLC.	cdf01e14-778b-4b3f-8372-1c18f266fb98	2025-08-06	Warnings, Adverse reactions	Exact identifier rxcui: 311197
Isosorbide Mononitrate	ISOSORBIDE MONONITRATE	Actavis Pharma, Inc.	ae8f74f0-e600-4452-8557-958b603e2709	2022-10-01	Warnings, Adverse reactions	Exact identifier rxcui: 311197
isosorbide mononitrate	ISOSORBIDE MONONITRATE	Lannett Company, Inc.	bf9e7e35-7707-42a0-88d6-6292fa52bbfa	2020-06-05	Warnings, Adverse reactions	Exact identifier rxcui: 311197
isosorbide mononitrate	ISOSORBIDE MONONITRATE	Proficient Rx LP	f871dfa7-219f-4704-8e4d-215caeb7408d	2019-11-01	Warnings, Adverse reactions	Exact identifier rxcui: 311197
B2D9550B-F025-568F-8FB4-0A77D16B1F64			EC09AB1C-52FA-4F41-BF65-A632DCE8F097	2007-03-31	Warnings, Adverse reactions	Exact identifier spl id: B2D9550B-F025-568F-8FB4-0A77D16B1F64 spl set id: EC09AB1C-52FA-4F41-BF65-A632DCE8F097

Reported adverse events (FAERS/openFDA)#

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