NDC 12634-177 Sulfamethoxazole And Trimethoprim Ds
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12634 - Apotheca Inc.
- 12634-177 - Sulfamethoxazole And Trimethoprim Ds
Product Characteristics
Product Packages
NDC Code 12634-177-00
Package Description: 10 TABLET in 1 BOTTLE
NDC Code 12634-177-59
Package Description: 30 TABLET in 1 BLISTER PACK
NDC Code 12634-177-71
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 12634-177-80
Package Description: 20 TABLET in 1 BOTTLE
NDC Code 12634-177-84
Package Description: 14 TABLET in 1 BOTTLE
NDC Code 12634-177-91
Package Description: 1 TABLET in 1 BLISTER PACK
NDC Code 12634-177-92
Package Description: 2 TABLET in 1 BOTTLE
NDC Code 12634-177-96
Package Description: 6 TABLET in 1 BOTTLE
Product Details
What is NDC 12634-177?
What are the uses for Sulfamethoxazole And Trimethoprim Ds?
Which are Sulfamethoxazole And Trimethoprim 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 Sulfamethoxazole And Trimethoprim 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
What is the NDC to RxNorm Crosswalk for Sulfamethoxazole And Trimethoprim Ds?
- RxCUI: 198335 - sulfamethoxazole 800 MG / trimethoprim 160 MG Oral Tablet
- RxCUI: 198335 - SMX 800 MG / TMP 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".