FDA.reportPublic FDA data

NDC 55999-085 - Sulfaplex

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
55999-085
Package NDCs from labels
55999-085-13, 55999-085-57, 55999-085-56, 55999-085-15, 55999-085-20
Manufacturer
Seachem Laboratories Inc.
Effective date
2018-07-16
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Sulfaplex™Seachem Laboratories Inc.2018-07-16OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55999-085-13Sulfaplex10 g in 1 VIAL, PLASTICPOWDER101
55999-085-15Sulfaplex100 g in 1 VIAL, PLASTICPOWDER1001
55999-085-20Sulfaplex4000 g in 1 VIAL, PLASTICPOWDER40001
55999-085-56Sulfaplex6 in 1 CASEPOWDER61
55999-085-57Sulfaplex1 in 1 CARTONPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55999-085SULFAPLEX (SULFATHIAZOLE) POWDER [SEACHEM LABORATORIES INC.]15 package rows20180723_638cfdf4-99cc-4c33-9144-ebadf96a9512.zip

Reported adverse events (FAERS/openFDA)#

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