NDC 21695-139 Butalbital, Aspirin, And Caffeine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-139 - Butalbital, Aspirin, And Caffeine
Product Characteristics
YELLOW (C48330 - YELLOW)
Product Packages
NDC Code 21695-139-60
Package Description: 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 21695-139?
What are the uses for Butalbital, Aspirin, And Caffeine?
Which are Butalbital, Aspirin, And Caffeine UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUTALBITAL (UNII: KHS0AZ4JVK)
- BUTALBITAL (UNII: KHS0AZ4JVK) (Active Moiety)
- ASPIRIN (UNII: R16CO5Y76E)
- ASPIRIN (UNII: R16CO5Y76E) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
Which are Butalbital, Aspirin, 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- GELATIN (UNII: 2G86QN327L)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Butalbital, Aspirin, And Caffeine?
- RxCUI: 238134 - butalbital 50 MG / aspirin 325 MG / caffeine 40 MG Oral Capsule
- RxCUI: 238134 - aspirin 325 MG / butalbital 50 MG / caffeine 40 MG Oral Capsule
- RxCUI: 238134 - ASA 325 MG / butalbital 50 MG / Caffeine 40 MG Oral Capsule
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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".