NDC 21695-777 Isosorbide Mononitrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
16 MM
KU;129;
1
Code Structure Chart
Product Details
What is NDC 21695-777?
What are the uses for Isosorbide Mononitrate?
Which are Isosorbide Mononitrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOSORBIDE MONONITRATE (UNII: LX1OH63030)
- ISOSORBIDE (UNII: WXR179L51S) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Isosorbide Mononitrate?
- RxCUI: 311196 - isosorbide mononitrate 120 MG 24HR Extended Release Oral Tablet
- RxCUI: 311196 - 24 HR isosorbide mononitrate 120 MG Extended Release Oral Tablet
- RxCUI: 311196 - isosorbide mononitrate 120 MG 24 HR Extended Release Oral Tablet
- RxCUI: 353538 - isosorbide mononitrate 60 MG 24HR Extended Release Oral Tablet
- RxCUI: 353538 - 24 HR isosorbide mononitrate 60 MG Extended Release Oral Tablet
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".