NDC 73309-126 - Sulfadiazine Base

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: 73309-126
Package NDCs from labels: 73309-126-01
Manufacturer: BLUEBAY SHANDONG CO.,LTD
Effective date: 2020-04-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Sulfadiazine Base - BLUEBAY SHANDONG CO.,LTD	BLUEBAY SHANDONG CO.,LTD	2020-04-21	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-126-01	Sulfadiazine Base	25 kg in 1 DRUM	POWDER	25		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-126	SULFADIAZINE BASE POWDER [BLUEBAY SHANDONG CO.,LTD]	1	1 package rows	20200422_47edee85-5713-467b-8f57-ec2dcdf3b254.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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
sulfADIAZINE	SULFADIAZINE	Chartwell RX, LLC	6032d6f7-cbce-4e5d-841c-a1e24b616f91	2024-09-24	Warnings, Adverse reactions	Exact identifier unii: 0N7609K889
SULFADIAZINE	SULFADIAZINE	EPIC PHARMA, LLC	8993651b-fff6-4e3f-9b60-78587bc9bcee	2023-11-08	Warnings, Adverse reactions	Exact identifier unii: 0N7609K889

Reported adverse events (FAERS/openFDA)#

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