NDC 0409-3412-01 - Meropenem

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: 0409-3412
Requested NDC: 0409-3412-01
Package NDCs from labels: 0409-3412-01, 0409-3412-10
Manufacturer: Hospira, Inc.
Effective date: 2024-11-06
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Meropenem - Hospira, Inc.	Hospira, Inc.	2024-11-06	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0409-3412-01	Meropenem	20 mL in 1 VIAL	INJECTION, POWDER, FOR SOLUTION	20		3
0409-3412-10	Meropenem	10 in 1 CARTON	INJECTION, POWDER, FOR SOLUTION	10		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0409-3412	MEROPENEM INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC.]	3	Current NDC, Legacy NDC, 2 package rows	20241108_e9b6555f-20a1-4415-bb80-3d034cfab95b.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0409-3412-01	EA - Each	0409-3412	49b0c34d-3928-40ac-9d31-913dca7def4f	1	2023-01-09
0409-3412-10	EA - Each	0409-3412	1cecb5c5-fe89-4220-95a1-fe0aff50c5ac	1	2023-01-09

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 2 of 2 · 23 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Meropenem	MEROPENEM	Fresenius Kabi USA, LLC	12714f80-d6e5-4453-b66c-62f57c16ddfc	2021-03-12	Warnings, Adverse reactions	Exact identifier application number: ANDA091404 rxcui: 1722934 rxcui: 1722939 unii: FV9J3JU8B1
Meropenem	MEROPENEM	Fresenius Kabi USA, LLC	7a68d899-2678-43a9-a9c1-ef8f916b562f	2021-03-10	Warnings, Adverse reactions	Exact identifier application number: ANDA091404 rxcui: 1722934 rxcui: 1722939 unii: FV9J3JU8B1
Meropenem	MEROPENEM	Fresenius Kabi USA, LLC	185181e3-c004-4d61-b992-5df94fe57a90	2020-10-19	Warnings, Adverse reactions	Exact identifier application number: ANDA091404 rxcui: 1722934 rxcui: 1722939 unii: FV9J3JU8B1

Reported adverse events (FAERS/openFDA)#

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