NDC 73057-357 Safety Coated Aspirin 325 Mg Regular Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73057 - Ulai Health Llc
- 73057-357 - Safety Coated Aspirin 325 Mg Regular Strength
Product Characteristics
Product Packages
NDC Code 73057-357-08
Package Description: 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 73057-357-11
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 73057-357?
What are the uses for Safety Coated Aspirin 325 Mg Regular Strength?
Which are Safety Coated Aspirin 325 Mg Regular Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
Which are Safety Coated Aspirin 325 Mg Regular Strength 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:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STARCH, CORN (UNII: O8232NY3SJ)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Safety Coated Aspirin 325 Mg Regular Strength?
- RxCUI: 198467 - aspirin 325 MG Delayed Release Oral Tablet
- RxCUI: 198467 - ASA 325 MG Delayed Release Oral Tablet
- RxCUI: 198467 - aspirin 325 MG Enteric Coated 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".