NDC 16590-210 Sulfamethoxazole And Trimethoprim

Product Information

Product Code16590-210
Proprietary Name What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Sulfamethoxazole And Trimethoprim
Product Labeler Information What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.
Stat Rx Usa Llc
Labeler Code16590
Start Marketing Date What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
01-25-2007
Listing Expiration Date 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.
12-31-2017
Exclude Flag 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".
I
NDC Code Structure

Usage Information


Product Characteristics

Color(s)WHITE (C48325 - TO OFF WHITE)
ShapeOVAL (C48345)
Size(s)19 MM
Imprint(s)5898;V
Score2

Product Packages

NDC 16590-210-10

Package Description: 10 TABLET in 1 BOTTLE, PLASTIC

NDC 16590-210-14

Package Description: 14 TABLET in 1 BOTTLE, PLASTIC

NDC 16590-210-15

Package Description: 15 TABLET in 1 BOTTLE, PLASTIC

NDC 16590-210-20

Package Description: 20 TABLET in 1 BOTTLE, PLASTIC

NDC 16590-210-28

Package Description: 28 TABLET in 1 BOTTLE, PLASTIC

NDC 16590-210-30

Package Description: 30 TABLET in 1 BOTTLE, PLASTIC

NDC 16590-210-40

Package Description: 40 TABLET in 1 BOTTLE, PLASTIC

NDC 16590-210-60

Package Description: 60 TABLET in 1 BOTTLE, PLASTIC

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Product Details

Sulfamethoxazole And Trimethoprim is product labeled by Stat Rx Usa Llc. The product's dosage form is and is administered via form.


What are Sulfamethoxazole And Trimethoprim Active Ingredients?

The following is the list of active ingredients in this product. An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.

  • SULFAMETHOXAZOLE (UNII: JE42381TNV)
  • SULFAMETHOXAZOLE (UNII: JE42381TNV) (Active Moiety)
  • TRIMETHOPRIM (UNII: AN164J8Y0X)
  • TRIMETHOPRIM (UNII: AN164J8Y0X) (Active Moiety)


NDC to RxNorm Crosswalk

What is RxNorm? RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct code indicates a single concept unique identifier (RXCUI) is associated with this product:


Inactive Ingredient(s)

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.

  • DOCUSATE SODIUM (UNII: F05Q2T2JA0)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • POVIDONE (UNII: FZ989GH94E)
  • STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)


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Patient Education

Co-trimoxazole

Co-trimoxazole is pronounced as (coe try mox' a zole)

Why is co-trimoxazole medication prescribed?
Co-trimoxazole is used to treat certain bacterial infections, such as pneumonia (a lung infection), bronchitis (infection of the tubes leading to the lungs), and infectio...
[Read More]

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Sulfamethoxazole And Trimethoprim Labeling and Warnings

FDA filings in the form of structured product labels are documents that include all published material associated whith this product. Product label information includes data like indications and usage generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

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