NDC11 00220065041

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
00220-0650-41	00220-0650
00220-650-41	00220-650
0220-0650-41	0220-0650

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
Aurum muriaticum natronatum	SODIUM TETRACHLOROAURATE	Boiron	8400a69a-fcd5-214b-e053-2991aa0a0f37	2023-11-08		Exact identifier ndc (package): 0220-0650-41 ndc (product): 0220-0650 ndc11 (package): 00220065041

Reported adverse events (FAERS/openFDA)#

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