FDA.reportPublic FDA data

NDC 43858-113-85 - 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
43858-113
Requested NDC
43858-113-85
Package NDCs from labels
43858-113-85, 43858-113-95
Manufacturer
Sandoz GmbH
Effective date
2017-08-15
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Ampicillin - Sandoz GmbHSandoz GmbH2017-08-15HUMAN PRESCRIPTION DRUG LABEL

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, 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
70093531-e996-4d0c-b5d0-9b74a8af713d70093531-e996-4d0c-b5d0-9b74a8af713d2017-08-15Warnings, Adverse reactionsExact identifier
spl id: 70093531-e996-4d0c-b5d0-9b74a8af713d
spl set id: 70093531-e996-4d0c-b5d0-9b74a8af713d

Reported adverse events (FAERS/openFDA)#

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