NDC 50383-338 Acetaminophen And Codeine Phosphate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50383 - Akorn
- 50383-338 - Acetaminophen And Codeine Phosphate
Product Details
What is NDC 50383-338?
What are the uses for Acetaminophen And Codeine Phosphate?
Which are Acetaminophen And Codeine Phosphate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ACETAMINOPHEN (UNII: 362O9ITL9D)
- ACETAMINOPHEN (UNII: 362O9ITL9D) (Active Moiety)
- CODEINE PHOSPHATE (UNII: GSL05Y1MN6)
- CODEINE ANHYDROUS (UNII: UX6OWY2V7J) (Active Moiety)
Which are Acetaminophen 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:
- ALCOHOL (UNII: 3K9958V90M)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- CHERRY (UNII: BUC5I9595W)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCROSE (UNII: C151H8M554)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Acetaminophen And Codeine Phosphate?
- RxCUI: 993755 - codeine phosphate 12 MG / acetaminophen 120 MG in 5 mL Oral Solution
- RxCUI: 993755 - acetaminophen 24 MG/ML / codeine phosphate 2.4 MG/ML Oral Solution
- RxCUI: 993755 - acetaminophen 120 MG / codeine phosphate 12 MG per 5 ML Oral Solution
- RxCUI: 993755 - acetaminophen 300 MG / codeine phosphate 30 MG per 12.5 ML Oral Solution
- RxCUI: 993755 - APAP 24 MG/ML / Codeine Phosphate 2.4 MG/ML Oral Solution
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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".