NDC 51808-204 Dipyridamole
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51808 - Anazaohealth Corporation
- 51808-204 - Dipyridamole
Product Characteristics
Product Packages
NDC Code 51808-204-01
Package Description: 10 mL in 1 VIAL
Product Details
What is NDC 51808-204?
What are the uses for Dipyridamole?
Which are Dipyridamole UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIPYRIDAMOLE (UNII: 64ALC7F90C)
- DIPYRIDAMOLE (UNII: 64ALC7F90C) (Active Moiety)
Which are Dipyridamole 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:
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
What is the NDC to RxNorm Crosswalk for Dipyridamole?
- RxCUI: 309953 - dipyridamole 50 MG in 10 ML Injection
- RxCUI: 309953 - 10 ML dipyridamole 5 MG/ML Injection
- RxCUI: 309953 - dipyridamole 50 MG per 10 ML Injection
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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".