NDC11 00220130641

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
00220-1306-41	00220-1306
0220-1306-41	0220-1306

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
Chininum sulphuricum	QUININE SULFATE	Boiron	8528ead8-9d2c-c708-e053-2a91aa0a0e1a	2023-11-09		Exact identifier ndc (package): 0220-1306-41 ndc (product): 0220-1306 ndc11 (package): 00220130641

Reported adverse events (FAERS/openFDA)#

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