NDC 53745-012 - Fritz Aquatics Mardel Maracyn Two

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
53745-012
Package NDCs from labels
53745-012-08, 53745-012-24, 53745-012-10, 53745-012-20, 53745-012-28
Manufacturer
Fritz Industries | Curia Italy S.r.l. | Sulzbach Enterprises, Inc.
Effective date
2024-01-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
fRITZ - Maracyn TwoFritz Industries | Curia Italy S.r.l. | Sulzbach Enterprises, Inc.2024-01-08OTC ANIMAL DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53745-012FRITZ AQUATICS MARDEL MARACYN TWO (MINOCYCLINE) POWDER [FRITZ INDUSTRIES]6Unmatched20240112_83cb77b3-d479-418d-9d7f-f6f060e9f225.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MINOCYCLINEACTIVE INGREDIENTFYY3R43WGOFRITZ AQUATICS MARDEL MARACYN TWO (MINOCYCLINE) POWDER [FRITZ INDUSTRIES]1
MINOCYCLINEACTIVE MOIETYFYY3R43WGOFRITZ AQUATICS MARDEL MARACYN TWO (MINOCYCLINE) POWDER [FRITZ INDUSTRIES]1

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 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ZILXIMINOCYCLINEJourney Medical Corporationcbffa96e-2446-43cf-ba5e-38c645302afd2024-02-09Warnings, Adverse reactionsName fallback
generic name: MINOCYCLINE
AMZEEQMINOCYCLINEJourney Medical Corporationcc251492-977b-4eb1-a088-a90831324bad2023-10-01Warnings, Adverse reactionsName fallback
generic name: MINOCYCLINE

Reported adverse events (FAERS/openFDA)#

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