NDC11 25021031720

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
25021-0317-20	25021-0317
25021-317-20	25021-317

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
labetalol hydrochloride	LABETALOL HYDROCHLORIDE	Sagent Pharmaceuticals	da8af6c2-d822-4ae5-9c2d-a1d161bdefd0	2022-04-12	Warnings, Adverse reactions	Exact identifier ndc (package): 25021-317-20 ndc (product): 25021-317 ndc11 (package): 25021031720

Reported adverse events (FAERS/openFDA)#

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