NDC 54868-0337 Bactrim Ds
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0337 - Bactrim Ds
Product Characteristics
Product Packages
NDC Code 54868-0337-0
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-0337-1
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 54868-0337-3
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-0337?
What are the uses for Bactrim Ds?
Which are Bactrim Ds 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 Bactrim Ds 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:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Bactrim Ds?
- RxCUI: 198335 - sulfamethoxazole 800 MG / trimethoprim 160 MG Oral Tablet
- RxCUI: 198335 - SMX 800 MG / TMP 160 MG Oral Tablet
- RxCUI: 849580 - Bactrim DS 800 MG/ 160 MG Oral Tablet
- RxCUI: 849580 - sulfamethoxazole 800 MG / trimethoprim 160 MG Oral Tablet [Bactrim]
- RxCUI: 849580 - Bactrim DS 800 MG / 160 MG Oral Tablet
* 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".