NDC 54868-2711 Isosorbide Dinitrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-2711 - Isosorbide Dinitrate
Product Characteristics
Product Packages
NDC Code 54868-2711-0
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 54868-2711-1
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 54868-2711-2
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-2711?
What are the uses for Isosorbide Dinitrate?
Which are Isosorbide Dinitrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ISOSORBIDE DINITRATE (UNII: IA7306519N)
- ISOSORBIDE (UNII: WXR179L51S) (Active Moiety)
Which are Isosorbide Dinitrate 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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Isosorbide Dinitrate?
- RxCUI: 311194 - isosorbide dinitrate 40 MG Extended Release Oral Tablet
- RxCUI: 311194 - ISDN 40 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".