FDA.reportPublic FDA data

NDC 76420-405 - Sulfamethoxazole and Trimethoprim

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
76420-405
Package NDCs from labels
76420-405-06, 76420-405-10, 76420-405-14, 76420-405-20, 76420-405-28, 76420-405-30, 76420-405-01, 76420-405-05
Manufacturer
ASCLEMED USA INC. | ASCLEMED USA INC. DBA ENOVACHEM
Effective date
2025-06-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DOCUSATE SODIUM - ASCLEMED USA INC. | ASCLEMED USA INC. DBA ENOVACHEMASCLEMED USA INC. | ASCLEMED USA INC. DBA ENOVACHEM2025-06-20HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
76420-405-01Sulfamethoxazole and Trimethoprim100 in 1 BOTTLETABLET1001
76420-405-05Sulfamethoxazole and Trimethoprim500 in 1 BOTTLETABLET5001
76420-405-06Sulfamethoxazole and Trimethoprim6 in 1 BOTTLETABLET61
76420-405-10Sulfamethoxazole and Trimethoprim10 in 1 BOTTLETABLET101
76420-405-14Sulfamethoxazole and Trimethoprim14 in 1 BOTTLETABLET141
76420-405-20Sulfamethoxazole and Trimethoprim20 in 1 BOTTLETABLET201
76420-405-28Sulfamethoxazole and Trimethoprim28 in 1 BOTTLETABLET281
76420-405-30Sulfamethoxazole and Trimethoprim30 in 1 BOTTLETABLET301

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 23 of 23 · 441 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
TrimethoprimTRIMETHOPRIMNovel Laboratories, Inc.b27e43b5-670b-43f6-b28b-413e54f914da2017-06-21Warnings, Adverse reactionsExact identifier
unii: AN164J8Y0X

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.