NDC 68405-298 Theracodophen-low-90
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PURPLE (C48327 - PURPLE WHITE)
21 MM
;
1
Code Structure Chart
Product Details
What is NDC 68405-298?
What are the uses for Theracodophen-low-90?
Which are Theracodophen-low-90 UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROCODONE BITARTRATE (UNII: NO70W886KK)
- HYDROCODONE (UNII: 6YKS4Y3WQ7) (Active Moiety)
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) (Active Moiety)
Which are Theracodophen-low-90 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- WHEY (UNII: 8617Z5FMF6)
- ARGININE (UNII: 94ZLA3W45F)
- HISTIDINE (UNII: 4QD397987E)
- GLUTAMINE (UNII: 0RH81L854J)
- CHOLINE BITARTRATE (UNII: 6K2W7T9V6Y)
- COCOA (UNII: D9108TZ9KG)
- THEOBROMINE (UNII: OBD445WZ5P)
- GRAPE (UNII: 6X543N684K)
- CINNAMON (UNII: 5S29HWU6QB)
- GELATIN (UNII: 2G86QN327L)
- TRICALCIUM PHOSPHATE (UNII: K4C08XP666)
- POWDERED CELLULOSE (UNII: SMD1X3XO9M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Theracodophen-low-90?
- RxCUI: 856903 - HYDROcodone bitartrate 5 MG / acetaminophen 500 MG Oral Tablet
- RxCUI: 856903 - acetaminophen 500 MG / hydrocodone bitartrate 5 MG Oral Tablet
- RxCUI: 856903 - APAP 500 MG / hydrocodone bitartrate 5 MG 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".