NDC 79739-7192 Butalbital, Aspirin, And Caffeine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 79739 - Lgm Pharma Solutions, Llc
- 79739-7192 - Butalbital, Aspirin, And Caffeine
Product Characteristics
BROWN (C48332 - BEIGE OPAQUE BODY)
Product Packages
NDC Code 79739-7192-1
Package Description: 100 CAPSULE in 1 BOTTLE
NDC Code 79739-7192-5
Package Description: 500 CAPSULE in 1 BOTTLE
Product Details
What is NDC 79739-7192?
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:
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Butalbital, Aspirin, And Caffeine?
- RxCUI: 2583731 - butalbital 50 MG / aspirin 500 MG / caffeine 40 MG Oral Capsule
- RxCUI: 2583731 - aspirin 500 MG / butalbital 50 MG / caffeine 40 MG Oral Capsule
- RxCUI: 2583731 - ASA 500 MG / butalbital 50 MG / caffeine 40 MG Oral Capsule
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Patient Education
Aspirin, Butalbital, and Caffeine
This combination of drugs is used to relieve tension headaches. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* 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".