NDC 10597-559 Fasprin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10597 - Nobel Laboratories, Llc
- 10597-559 - Fasprin
Product Characteristics
Product Packages
NDC Code 10597-559-05
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BOX
NDC Code 10597-559-06
Package Description: 100 TABLET, ORALLY DISINTEGRATING in 1 BOX
Product Details
What is NDC 10597-559?
What are the uses for Fasprin?
Which are Fasprin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Fasprin 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:
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CROSPOVIDONE (UNII: 68401960MK)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- GLUCOSAMINE (UNII: N08U5BOQ1K)
- MANNITOL (UNII: 3OWL53L36A)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- SORBITOL (UNII: 506T60A25R)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
What is the NDC to RxNorm Crosswalk for Fasprin?
- RxCUI: 747211 - aspirin 81 MG Disintegrating Oral Tablet
- RxCUI: 747211 - ASA 81 MG Disintegrating Oral Tablet
- RxCUI: 747236 - FASPRIN 81 MG Disintegrating Oral Tablet
- RxCUI: 747236 - aspirin 81 MG Disintegrating Oral Tablet [Fasprin]
- RxCUI: 747236 - ASA 81 MG Disintegrating Oral Tablet [Fasprin]
* 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".