NDC11 71288060092

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
71288-0600-92	71288-0600
71288-600-92	71288-600

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
Pantoprazole Sodium	PANTOPRAZOLE SODIUM	Meitheal Pharmaceuticals Inc.	014f9762-6948-46b7-8659-5c89f35ad8bf	2025-06-27	Warnings, Adverse reactions	Exact identifier ndc (package): 71288-600-92 ndc (product): 71288-600 ndc11 (package): 71288060092
Pantoprazole Sodium	PANTOPRAZOLE SODIUM	Meitheal Pharmaceuticals Inc.	c18aff31-f91e-4b6a-9713-52c9094c6082	2025-03-13	Warnings, Adverse reactions	Exact identifier ndc (product): 71288-600

Reported adverse events (FAERS/openFDA)#

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