NDC11 71288042691

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
71288-0426-91	71288-0426
71288-426-91	71288-426

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Enoxaparin Sodium	ENOXAPARIN SODIUM	Meitheal Pharmaceuticals Inc.	7d38c307-767f-4c38-ac0e-b8bb62782602	2024-12-06	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 71288-426
Enoxaparin Sodium	ENOXAPARIN SODIUM	Meitheal Pharmaceuticals Inc.	adfc2b23-00a5-4f05-a08b-83087e1e4843	2024-02-05	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 71288-426-91 ndc (product): 71288-426 ndc11 (package): 71288042691

Reported adverse events (FAERS/openFDA)#

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