NDC11 65197020309

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
65197-0203-09	65197-0203
65197-0203-9	65197-0203
65197-203-09	65197-203

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
Emetrol Powder Non-Drowsy	SODIUM CITRATE DIHYDRATE	WellSpring Pharmaceutical Corporation	9d8d2ee7-9db7-4be7-8c73-511eb2e32459	2025-01-08	Warnings	Exact identifier ndc (package): 65197-203-09 ndc (product): 65197-203 ndc11 (package): 65197020309

Reported adverse events (FAERS/openFDA)#

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