NDC 50090-0962 Digox
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50090 - A-s Medication Solutions
- 50090-0962 - Digox
Product Characteristics
Product Packages
NDC Code 50090-0962-1
Package Description: 100 TABLET in 1 BOTTLE
Product Details
What is NDC 50090-0962?
What are the uses for Digox?
Which are Digox UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIGOXIN (UNII: 73K4184T59)
- DIGOXIN (UNII: 73K4184T59) (Active Moiety)
Which are Digox 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)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Digox?
- RxCUI: 1245373 - Digox 250 MCG Oral Tablet
- RxCUI: 1245373 - digoxin 0.25 MG Oral Tablet [Digox]
- RxCUI: 1245373 - Digox 0.25 MG Oral Tablet
- RxCUI: 197606 - digoxin 250 MCG Oral Tablet
- RxCUI: 197606 - digoxin 0.25 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Digoxin
Digoxin is used to treat heart failure and abnormal heart rhythms (arrhythmias). It helps the heart work better and it helps control your heart rate.
[Learn More]
* 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".