NDC11 25021030566

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
25021-0305-66	25021-0305
25021-305-66	25021-305

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
chlorothiazide sodium	CHLOROTHIAZIDE SODIUM	Sagent Pharmaceuticals	377dc515-e381-4196-8bc7-b738606c57ac	2026-08-04	Warnings, Adverse reactions	Exact identifier ndc (product): 25021-305
chlorothiazide sodium	CHLOROTHIAZIDE SODIUM	Sagent Pharmaceuticals	82dd0bdd-e6bd-48ea-8f58-c8bf71bbfe2c	2026-08-04	Warnings, Adverse reactions	Exact identifier ndc (package): 25021-305-66 ndc (product): 25021-305 ndc11 (package): 25021030566

Reported adverse events (FAERS/openFDA)#

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