NDC11 69727000201

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
69727-0002-01	69727-0002
69727-0002-1	69727-0002
69727-002-01	69727-002

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
Ultra Advantage	ABROTANUM (ARTEMISIA ABROTANUM), ANACARDIUM ORIENTALE, FUCUS VESICULOSUS, HELLEBORUS NIGER, HYPOTHALAMUS SUIS, LYCOPODIUM CLAVATUM, THYMOLUM, THYMUS SERPYLLUM, THYROIDINUM (BOVINE), GLANDULA SUPRARENALIS SUIS, HEPAR SUIS, PANCREAS SUIS, CINCHONA OFFICINALIS, GRAPHITES, NICOTINAMIDUM, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, MAGNESIA PHOSPHORICA, SOLIDAGO VIRGAUREA	ELTTAC Inc DBA SWL	5038034c-93f5-4b42-945d-0a6d2a58e0cb	2018-12-12	Warnings	Exact identifier ndc (package): 69727-0002-1 ndc (product): 69727-0002 ndc11 (package): 69727000201

Reported adverse events (FAERS/openFDA)#

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