FDA.reportPublic FDA data

NDC 17156-525-01 - DMSA

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
17156-525
Requested NDC
17156-525-01
Package NDCs from labels
17156-525-01
Manufacturer
GE Healthcare
Effective date
2007-08-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
DMSA - GE HealthcareGE Healthcare2007-08-03HUMAN PRESCRIPTION DRUG LABELING

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
17156-525-01DMSA5 in 1 BOXINJECTION, POWDER, LYOPHILIZED,52
17156-525-01DMSA1 in 1 VIALINJECTION, POWDER, LYOPHILIZED,12

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
17156-525DMSA (DIMERCAPTOSUCCINIC ACID) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GE HEALTHCARE]22 package rows20071017_ADB26DA0-5494-4EAB-975B-A1954A995AE8.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Dimercaptocuccinic AcidACTIVE INGREDIENT4S9JU7XF01DMSA (DIMERCAPTOSUCCINIC ACID) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GE HEALTHCARE]2
Dimercaptocuccinic AcidACTIVE MOIETY4S9JU7XF01DMSA (DIMERCAPTOSUCCINIC ACID) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GE HEALTHCARE]2
ascorbic acidINACTIVE INGREDIENTPQ6CK8PD0RDMSA (DIMERCAPTOSUCCINIC ACID) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GE HEALTHCARE]2
inositolINACTIVE INGREDIENT4L6452S749DMSA (DIMERCAPTOSUCCINIC ACID) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GE HEALTHCARE]2
Stannous Chloride DihydrateINACTIVE INGREDIENT1BQV3749L5DMSA (DIMERCAPTOSUCCINIC ACID) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [GE HEALTHCARE]2

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 ยท 5 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Ascorbic AcidASCORBIC ACIDRenova Pharmaceuticals LLCa6481bae-2397-44c7-a51d-4f47ad91bd2c2026-08-19Warnings, Adverse reactionsName fallback
brand name: Ascorbic Acid
CLARISCANGADOTERATE MEGLUMINEGE Healthcarec9e273b3-481f-4899-8913-95aaddcc76622026-04-30Boxed warning, Warnings, Adverse reactionsName fallback
manufacturer name: GE Healthcare
CLARISCANGADOTERATE MEGLUMINEGE Healthcare6f8c9fac-c995-4bf4-950d-ab89deb291b52026-04-29Boxed warning, Warnings, Adverse reactionsName fallback
manufacturer name: GE Healthcare
OmnipaqueIOHEXOLGE Healthcare164b27b9-97ae-4279-896f-1c4afa583dd12026-04-07Boxed warning, Warnings, Adverse reactionsName fallback
manufacturer name: GE Healthcare
Ascorbic AcidASCORBIC ACIDFresenius Kabi USA, LLC1606e29f-0e80-4069-b688-daab9cbff20a2025-12-17Warnings, Adverse reactionsName fallback
brand name: Ascorbic Acid

Reported adverse events (FAERS/openFDA)#

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