NDC11 71753201301

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
71753-2013-01	71753-2013
71753-2013-1	71753-2013

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
Allergy Escape	ALLIUM CEPA, EUPHRASIA OFFICINALIS, KALI IODATUM, NAPHTHALINUM, SABADILLA, URTICA URENS, WYETHIA HELENIOIDES, HISTAMINUM HYDROCHLORICUM	Ratis, LLC	8bd9b9da-570a-4875-a5de-963155f0f837	2023-07-12	Warnings	Exact identifier ndc (package): 71753-2013-1 ndc (product): 71753-2013 ndc11 (package): 71753201301

Reported adverse events (FAERS/openFDA)#

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