NDC 73309-303-01 - Sevelamer Carbonate

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: 73309-303
Requested NDC: 73309-303-01
Package NDCs from labels: 73309-303-01
Manufacturer: Bluebay Shangdong Co.,LTD
Effective date: 2021-06-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Sevelamer Carbonate - Bluebay Shangdong Co.,LTD	Bluebay Shangdong Co.,LTD	2021-06-17	BULK INGREDIENT

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
73309-303-01	Sevelamer Carbonate	500 g in 1 JAR	POWDER	500		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
73309-303	SEVELAMER CARBONATE POWDER [BLUEBAY SHANGDONG CO.,LTD]	1	1 package rows	20210618_9bf4b8fb-f1ea-4155-94a5-c04410d3edd9.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 3 of 3 · 42 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Sevelamer carbonate	SEVELAMER CARBONATE	Cipla USA Inc.	f63450bd-d075-4810-a277-e8bc41e4a5af	2018-12-19	Warnings, Adverse reactions	Exact identifier unii: 9YCX42I8IU
Sevelamer carbonate	SEVELAMER CARBONATE	Exelan Pharmaceuticals Inc.	568b8558-6117-4c2f-aabf-86e567b38863	2018-11-29	Warnings, Adverse reactions	Exact identifier unii: 9YCX42I8IU

Reported adverse events (FAERS/openFDA)#

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