NDC 71335-0762 – Sulfamethoxazole and Trimethoprim

Sulfamethoxazole 800 mg/1; Trimethoprim 160 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0762

Product details

Brand name
Sulfamethoxazole and Trimethoprim
Generic name
Sulfamethoxazole and Trimethoprim
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090624
Marketed since
February 16, 2010
Listing expires
December 31, 2026
Pharmacologic class
Dihydrofolate Reductase Inhibitor Antibacterial; Sulfonamide Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Sulfamethoxazole and Trimethoprim →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0762-021 TABLET in 1 BOTTLE (71335-0762-0)Jul 24, 2020
71335-0762-120 TABLET in 1 BOTTLE (71335-0762-1)Jun 19, 2018
71335-0762-214 TABLET in 1 BOTTLE (71335-0762-2)Apr 5, 2018
71335-0762-310 TABLET in 1 BOTTLE (71335-0762-3)Mar 29, 2018
71335-0762-428 TABLET in 1 BOTTLE (71335-0762-4)Mar 26, 2018
71335-0762-540 TABLET in 1 BOTTLE (71335-0762-5)Apr 24, 2018
71335-0762-66 TABLET in 1 BOTTLE (71335-0762-6)Nov 4, 2019
71335-0762-760 TABLET in 1 BOTTLE (71335-0762-7)Nov 10, 2020
71335-0762-830 TABLET in 1 BOTTLE (71335-0762-8)Jun 18, 2018
71335-0762-913 TABLET in 1 BOTTLE (71335-0762-9)Oct 7, 2024

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