60429-258 NDC - SULFAMETHOXAZOLE AND TRIMETHOPRIM ()

Drug Information

  • Product NDC: 60429-258
  • Proprietary Name: Sulfamethoxazole and Trimethoprim
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Golden State Medical Supply, Inc.
Product Type:
FDA Application Number: ANDA071017
Marketing Category: ANDA
Start Marketing Date:8/25/1986
End Marketing Date:9/30/2018

Package Information

No. Package Code Package Description Billing Unit
160429-258-01100 TABLET in 1 BOTTLE, PLASTIC (60429-258-01)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC60429-258The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMESulfamethoxazole and TrimethoprimThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/25/1986This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE9/30/2018The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
MARKETING CATEGORY NAMEANDAThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
APPLICATION NUMBERANDA071017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGolden State Medical Supply, Inc.This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.

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This page was last updated on: 11/21/2025

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