NDC11 00703951401

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDC	Product root
00703-9514-01	00703-9514
00703-9514-1	00703-9514
0703-9514-01	0703-9514

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 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sulfamethoxazole and Trimethoprim	SULFAMETHOXAZOLE AND TRIMETHOPRIM	Teva Parenteral Medicines, Inc.	bf7a0845-de4f-46be-841a-0faf47f8b530	2025-04-30	Warnings, Adverse reactions	Exact identifier ndc (product): 0703-9514
Sulfamethoxazole and Trimethoprim	SULFAMETHOXAZOLE AND TRIMETHOPRIM	Teva Parenteral Medicines, Inc.	b89b5502-ce87-45a6-a43c-9891da3cfca4	2025-04-30	Warnings, Adverse reactions	Exact identifier ndc (package): 0703-9514-01 ndc (product): 0703-9514 ndc11 (package): 00703951401
Sulfamethoxazole and Trimethoprim	SULFAMETHOXAZOLE AND TRIMETHOPRIM	Teva Parenteral Medicines, Inc.	640f5b0c-748d-4a68-a1de-59cc3e00ed49	2025-04-30	Warnings, Adverse reactions	Exact identifier ndc (product): 0703-9514

Reported adverse events (FAERS/openFDA)#

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