Amikacin Sulfate Injection, 500 mg/2ml

Manufacturer
Prodigy Innovation, LLC.
Effective date
2019-05-05
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 20:28:35

Label at a glance#

ProductAmikacin Sulfate Injection, 500 mg/2ml
Active ingredientAMIKACIN SULFATE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1598047amikacin 250 MG/ML Injectable SolutionSCD1
1598047amikacin (as amikacin sulfate) 250 MG/ML Injectable SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
AMIKACIN Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
e1d8d349-40e8-4ab6-9f36-aa84681732edProduct name320250124
7a2acf42-1a2f-4e31-9d74-f6d541e9bb46Product name120190111
37302fde-6a8c-4412-a7e0-b0fdb78cc567Product name120151215
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70297-996-052021-01-29C16284748780-1ba0f9c33-26bc-a910-e053-dadaa90a0b85Amikacin Sulfate Injection, 500 mg / 2ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70297-996-05Amikacin Sulfate Injection, 500 mg/2ml500 in 1 BOTTLEINJECTION5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70297-996AMIKACIN SULFATE INJECTION, 500 MG/2ML INJECTION [PRODIGY INNOVATION, LLC.]11 package rows20190506_882c39a9-2198-9063-e053-2995a90af7ad.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70297-99670297-996-05

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
882c39a9-2197-9063-e053-2995a90af7ad882c39a9-2198-9063-e053-2995a90af7ad2019-05-05Exact identifier
spl id: 882c39a9-2197-9063-e053-2995a90af7ad
spl set id: 882c39a9-2198-9063-e053-2995a90af7ad

Reported adverse events (FAERS/openFDA)#

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