NDC 17856-5181 Sulfamethoxazole And Trimethoprim
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 17856-5181?
What are the uses for Sulfamethoxazole And Trimethoprim?
Which are Sulfamethoxazole And Trimethoprim UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFAMETHOXAZOLE (UNII: JE42381TNV)
- SULFAMETHOXAZOLE (UNII: JE42381TNV) (Active Moiety)
- TRIMETHOPRIM (UNII: AN164J8Y0X)
- TRIMETHOPRIM (UNII: AN164J8Y0X) (Active Moiety)
Which are Sulfamethoxazole And Trimethoprim 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)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- WATER (UNII: 059QF0KO0R)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SORBITOL (UNII: 506T60A25R)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
What is the NDC to RxNorm Crosswalk for Sulfamethoxazole And Trimethoprim?
- RxCUI: 313134 - sulfamethoxazole 200 MG / trimethoprim 40 MG in 5 mL Oral Suspension
- RxCUI: 313134 - sulfamethoxazole 40 MG/ML / trimethoprim 8 MG/ML Oral Suspension
- RxCUI: 313134 - SMX 40 MG/ML / TMP 8 MG/ML Oral Suspension
- RxCUI: 313134 - sulfamethoxazole 100 MG / trimethoprim 20 MG per 2.5 ML Oral Suspension
- RxCUI: 313134 - sulfamethoxazole 200 MG / trimethoprim 40 MG per 5 ML Oral Suspension
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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".