FDA.reportPublic FDA data

NDC 0409-3718-10 - Ampicillin

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
0409-3718
Requested NDC
0409-3718-10
Package NDCs from labels
0409-3718-10, 0409-3718-01
Manufacturer
Hospira, Inc
Effective date
2024-05-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ampicillin - Hospira, IncHospira, Inc2024-05-08HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0409-3718-01EA - Each0409-3718b1e0c1a9-e702-44c8-b5fa-55bc0236423f12017-09-11
0409-3718-10EA - Each0409-371803c53ffb-8c63-42fd-8f88-5e08d8eea5d312017-09-11

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 4 of 4 · 63 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AmpicillinAMPICILLINMedical Purchasing Solutions, LLCbbf118c0-7cd3-5a82-e053-2a95a90ac8c82023-05-08Warnings, Adverse reactionsExact identifier
unii: JFN36L5S8K
AmpicillinAMPICILLINMedical Purchasing Solutions, LLCc4310ee5-cbd3-99b5-e053-2995a90ae2292023-04-27Warnings, Adverse reactionsExact identifier
unii: JFN36L5S8K
AmpicillinAMPICILLIN SODIUMFresenius Kabi USA, LLC8dbb4c71-8543-08f1-e053-2995a90af88d2022-10-21Warnings, Adverse reactionsExact identifier
unii: JFN36L5S8K

Reported adverse events (FAERS/openFDA)#

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