FDA.reportPublic FDA data

NDC 55999-057-52 - Cupramine

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
55999-057
Requested NDC
55999-057-52
Package NDCs from labels
55999-057-00, 55999-057-63, 55999-057-01, 55999-057-60, 55999-057-03, 55999-057-62, 55999-057-06, 55999-057-58, 55999-057-08, 55999-057-54, 55999-057-09, 55999-057-52, 55999-057-10
Manufacturer
Seachem Laboratories Inc.
Effective date
2019-08-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cupramine™Seachem Laboratories Inc.2019-08-07OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55999-057-00Cupramine50 mL in 1 BOTTLE, PLASTICLIQUID502
55999-057-01Cupramine100 mL in 1 BOTTLE, PLASTICLIQUID1002
55999-057-03Cupramine250 mL in 1 BOTTLE, PLASTICLIQUID2502
55999-057-06Cupramine500 mL in 1 BOTTLE, PLASTICLIQUID5002
55999-057-08Cupramine2000 mL in 1 BOTTLE, PLASTICLIQUID20002
55999-057-09Cupramine4000 mL in 1 BOTTLE, PLASTICLIQUID40002
55999-057-10Cupramine20000 mL in 1 BOTTLE, PLASTICLIQUID200002
55999-057-52Cupramine2 in 1 CASELIQUID22
55999-057-54Cupramine4 in 1 CASELIQUID42
55999-057-58Cupramine12 in 1 CASELIQUID122
55999-057-60Cupramine25 in 1 CASELIQUID252
55999-057-62Cupramine25 in 1 CASELIQUID252
55999-057-63Cupramine25 in 1 CASELIQUID252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55999-057CUPRAMINE (CUPRIC SULFATE ANHYDROUS) LIQUID [SEACHEM LABORATORIES INC.]213 package rows20190815_a5062dac-94f8-434b-93ca-b087f902afe0.zip

Reported adverse events (FAERS/openFDA)#

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