NDC 16590-022 Acetaminophen, Butalbital And Caffeine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-022 - Acetaminophen, Butalbital And Caffeine
Product Characteristics
Product Packages
NDC Code 16590-022-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC
NDC Code 16590-022-20
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC
NDC Code 16590-022-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 16590-022-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 16590-022-72
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
NDC Code 16590-022-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
NDC Code 16590-022-99
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 16590-022?
What are the uses for Acetaminophen, Butalbital And Caffeine?
Which are Acetaminophen, Butalbital And Caffeine UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- BUTALBITAL (UNII: KHS0AZ4JVK)
- BUTALBITAL (UNII: KHS0AZ4JVK) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
Which are Acetaminophen, Butalbital And Caffeine 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
What is the NDC to RxNorm Crosswalk for Acetaminophen, Butalbital And Caffeine?
- RxCUI: 238154 - butalbital 50 MG / acetaminophen 325 MG / caffeine 40 MG Oral Tablet
- RxCUI: 238154 - acetaminophen 325 MG / butalbital 50 MG / caffeine 40 MG Oral Tablet
- RxCUI: 238154 - APAP 325 MG / butalbital 50 MG / caffeine 40 MG 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".