NDC 76000-231 Aspirin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 76000-231-12
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 120 TABLET in 1 BOTTLE, PLASTIC
NDC Code 76000-231-15
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 150 TABLET in 1 BOTTLE, PLASTIC
NDC Code 76000-231-20
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 200 TABLET in 1 BOTTLE, PLASTIC
NDC Code 76000-231-30
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 300 TABLET in 1 BOTTLE, PLASTIC
NDC Code 76000-231-36
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 36 TABLET in 1 BOTTLE, PLASTIC
NDC Code 76000-231-65
Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 365 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 76000-231?
What are the uses for Aspirin?
Which are Aspirin UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Aspirin 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:
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Aspirin?
- RxCUI: 308416 - aspirin 81 MG Delayed Release Oral Tablet
- RxCUI: 308416 - ASA 81 MG Delayed Release Oral Tablet
- RxCUI: 308416 - aspirin 81 MG Enteric Coated 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".