NDC 71740-010-42 - Protyl Ag

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 71740-010
Requested NDC: 71740-010-42
Package NDCs from labels: 71740-010-42
Manufacturer: Avondale Pharmaceuticals, LLC
Effective date: 2022-03-11
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Protyl Ag - Avondale Pharmaceuticals, LLC	Avondale Pharmaceuticals, LLC	2022-03-11	PRESCRIPTION MEDICAL DEVICE LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
71740-010-42	GM - Gram	71740-010	f50cf9ac-f051-4658-a752-106d0b648bfa	1	2019-04-11

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
SSKI	POTASSIUM IODIDE	Avondale Pharmaceuticals, LLC	ca1d3449-ea29-49a4-8863-365ec95f1553	2025-07-09	Warnings, Adverse reactions	Name fallback manufacturer name: Avondale Pharmaceuticals, LLC
Niacor	NIACIN	Avondale Pharmaceuticals, LLC	bf287412-160b-403f-8eb4-57f29a475902	2021-12-23	Warnings, Adverse reactions	Name fallback manufacturer name: Avondale Pharmaceuticals, LLC

Reported adverse events (FAERS/openFDA)#

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