NDC 68258-2012 Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68258 - Dispensing Solutions, Inc.
- 68258-2012 - Butalbital, Acetaminophen, Caffeine And Codeine Phosphate
Product Characteristics
GRAY (C48324)
Product Packages
NDC Code 68258-2012-9
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 68258-2012?
What are the uses for Butalbital, Acetaminophen, Caffeine And Codeine Phosphate?
Which are Butalbital, Acetaminophen, Caffeine And Codeine Phosphate UNII Codes?
The UNII codes for the active ingredients in this product are:
- BUTALBITAL (UNII: KHS0AZ4JVK)
- BUTALBITAL (UNII: KHS0AZ4JVK) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CAFFEINE (UNII: 3G6A5W338E)
- CAFFEINE (UNII: 3G6A5W338E) (Active Moiety)
- CODEINE PHOSPHATE (UNII: GSL05Y1MN6)
- CODEINE (UNII: Q830PW7520) (Active Moiety)
Which are Butalbital, Acetaminophen, Caffeine And Codeine Phosphate 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 BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- GELATIN (UNII: 2G86QN327L)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Butalbital, Acetaminophen, Caffeine And Codeine Phosphate?
- RxCUI: 993943 - butalbital 50 MG / acetaminophen 325 MG / caffeine 40 MG / codeine phosphate 30 MG Oral Capsule
- RxCUI: 993943 - acetaminophen 325 MG / butalbital 50 MG / caffeine 40 MG / codeine phosphate 30 MG Oral Capsule
- RxCUI: 993943 - APAP 325 MG / butalbital 50 MG / caffeine 40 MG / codeine phosphate 30 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".