NDC 54868-4417 Isosorbide Mononitrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4417 - Isosorbide Mononitrate
Product Characteristics
15 MM
KU;119;
Product Packages
NDC Code 54868-4417-0
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 54868-4417-1
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 54868-4417-2
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-4417?
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 MONONITRATE (UNII: LX1OH63030) (Active Moiety)
- ISOSORBIDE (UNII: WXR179L51S) (Active Moiety)
Which are Isosorbide Mononitrate Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TALC (UNII: 7SEV7J4R1U)
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: 317110 - isosorbide mononitrate 30 MG 24HR Extended Release Oral Tablet
- RxCUI: 317110 - 24 HR isosorbide mononitrate 30 MG Extended Release Oral Tablet
* Please review the disclaimer below.
[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".