NDC11 63323065827

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
63323-0658-27	63323-0658
63323-658-27	63323-658

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
Chlorothiazide	CHLOROTHIAZIDE SODIUM	Fresenius Kabi USA, LLC	5b5d8a97-1428-4047-8e6c-b778429a26e4	2026-01-08	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-658
Chlorothiazide	CHLOROTHIAZIDE SODIUM	Fresenius Kabi USA, LLC	de512e9b-444c-4ae4-8c6b-accd87a02021	2025-03-20	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-658
Chlorothiazide	CHLOROTHIAZIDE SODIUM	Fresenius Kabi USA, LLC	de250776-461a-4d02-a82e-ffedca1a9cf4	2023-06-02	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-658-27 ndc (product): 63323-658 ndc11 (package): 63323065827

Reported adverse events (FAERS/openFDA)#

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