MedPath

Sulfamethoxazole and Trimethoprim

Approved
Approval ID

3fc95839-6b77-1303-e054-00144ff88e88

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 19, 2022

Manufacturers
FDA

RedPharm Drug, Inc.

DUNS: 828374897

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

Sulfamethoxazole and Trimethoprim

PRODUCT DETAILS

NDC Product Code67296-0227
Application NumberANDA076899
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 19, 2022
Generic NameSulfamethoxazole and Trimethoprim

INGREDIENTS (6)

MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
SULFAMETHOXAZOLEActive
Quantity: 800 mg in 1 1
Code: JE42381TNV
Classification: ACTIB
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
SODIUM STARCH GLYCOLATE TYPE A POTATOInactive
Code: 5856J3G2A2
Classification: IACT
TRIMETHOPRIMActive
Quantity: 160 mg in 1 1
Code: AN164J8Y0X
Classification: ACTIB
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
© Copyright 2025. All Rights Reserved by MedPath
Sulfamethoxazole and Trimethoprim - FDA Approval | MedPath