Home NDC 0409-2987-23 NDC 0409-2987-23 - Ampicillin and Sulbactam 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 0409-2987
Requested NDC 0409-2987-23
Package NDCs from labels 0409-2987-23, 0409-2987-03
Manufacturer Hospira, Inc
Effective date 2026-01-21
Current FDA listing Not matched in FDA.report NDC product tables
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 0409-2987-03 Ampicillin and Sulbactam 10 in 1 TRAY INJECTION, POWDER, FOR SOLUTION 10 23 0409-2987-23 Ampicillin and Sulbactam 1 in 1 VIAL INJECTION, POWDER, FOR SOLUTION 1 23
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 0409-2987 AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM) INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC] 22 Current NDC, Legacy NDC, 2 package rows 20240828_dc374fa4-350b-425d-a7db-7099fdc64cf1.zip
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded AMPICILLIN SODIUM ACTIVE INGREDIENT JFN36L5S8K AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM) INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC] 11 SULBACTAM SODIUM ACTIVE INGREDIENT DKQ4T82YE6 AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM) INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC] 11 AMPICILLIN ACTIVE MOIETY 7C782967RD AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM) INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC] 11 SULBACTAM ACTIVE MOIETY S4TF6I2330 AMPICILLIN AND SULBACTAM (AMPICILLIN SODIUM AND SULBACTAM SODIUM) INJECTION, POWDER, FOR SOLUTION [HOSPIRA, INC] 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 · 62 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.