NDC 54868-0337-0 Bactrim Ds

Package Information

What is NDC 54868-0337-0?

The NDC Code 54868-0337-0 is assigned to a package of 20 tablet in 1 bottle, plastic of Bactrim Ds, labeled by Physicians Total Care, Inc.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 20 billable units per package. The following table has all the important details about this NDC code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

Field Name Field Value
NDC Code 54868-0337-0
Package Description 20 TABLET in 1 BOTTLE, PLASTIC
Product Code 54868-0337
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.
Bactrim Ds
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
This medication is a combination of two antibiotics: sulfamethoxazole and trimethoprim. It is used to treat a wide variety of bacterial infections (such as middle ear, urine, respiratory, and intestinal infections). It is also used to prevent and treat a certain type of pneumonia (pneumocystis-type). This medication should not be used in children less than 2 months of age due to the risk of serious side effects. This medication treats only certain types of infections. It will not work for viral infections (such as flu). Unnecessary use or misuse of any antibiotic can lead to its decreased effectiveness.
11-Digit NDC Billing Format NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
54868033700
Billing Unit EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Estimated Billable Units per Package 20 EA
NDC to RxNorm Crosswalk
  • 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
  • Labeler Name Physicians Total Care, Inc.
    Sample Package Sample Package?
    This field Indicates whether this package is a sample packaging or not.
    No
    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.
    08-26-1997
    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
    This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for Bactrim Ds with product NDC 54868-0337.

    NDC Package CodePackage Description
    54868-0337-130 TABLET in 1 BOTTLE, PLASTIC
    54868-0337-310 TABLET in 1 BOTTLE, PLASTIC

    * Please review the disclaimer below.