NDC 59051-9075 - RenaKare

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
59051-9075
Package NDCs from labels
59051-9075-1
Manufacturer
Neogen Corporation-Mercer Rd | Jungbunzlauer Ladenburg GmbH
Effective date
2023-02-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
RenaKare - Neogen Corporation-Mercer Rd | Jungbunzlauer Ladenburg GmbHNeogen Corporation-Mercer Rd | Jungbunzlauer Ladenburg GmbH2023-02-21PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
59051-9075-1RenaKare113 g in 1 BOTTLE, PLASTICPOWDER1133

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
59051-9075RENAKARE (POTASSIUM GLUCONATE) POWDER [NEOGEN CORPORATION-MERCER RD]31 package rows20230222_af6cbe7b-bdb7-49c5-9ec1-ac3942889366.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
POTASSIUM GLUCONATEACTIVE INGREDIENT12H3K5QKN9RENAKARE (POTASSIUM GLUCONATE) POWDER [NEOGEN CORPORATION-MERCER RD]1
POTASSIUM CATIONACTIVE MOIETY295O53K152RENAKARE (POTASSIUM GLUCONATE) POWDER [NEOGEN CORPORATION-MERCER RD]1