NDC 73309-018 - Paromomycin Sulfate

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: 73309-018
Package NDCs from labels: 73309-018-01
Manufacturer: BLUEBAY SHANDONG CO.,LTD
Effective date: 2019-08-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Paromomycin Sulfate - BLUEBAY SHANDONG CO.,LTD	BLUEBAY SHANDONG CO.,LTD	2019-08-21	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-018-01	Paromomycin Sulfate	1 kg in 1 JAR	POWDER	1		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-018	PAROMOMYCIN SULFATE POWDER [BLUEBAY SHANDONG CO.,LTD]	1	1 package rows	20190822_6c2b9fe3-c1f9-478a-af17-70b8dacedfdb.zip

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
Humatin	PAROMOMYCIN SULFATE	Waylis Therapeutics LLC	a725f022-ec3c-430d-8021-96c861b9893c	2025-11-13	Adverse reactions	Exact identifier unii: 845NU6GJPS

Reported adverse events (FAERS/openFDA)#

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