NDC 50989-181 - ClindaCure

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
50989-181
Package NDCs from labels
50989-181-09
Manufacturer
VEDCO | FIRST PRIORITY INCORPORATED
Effective date
2024-12-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
ClindaCure - VEDCO | FIRST PRIORITY INCORPORATEDVEDCO | FIRST PRIORITY INCORPORATED2024-12-09PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50989-181-09ClindaCure12 in 1 CASELIQUID1211
50989-181-09ClindaCure1 in 1 CARTONLIQUID111

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50989-181CLINDACURE (CLINAMYCIN HYDROCHLORIDE) LIQUID [VEDCO]112 package rows20241211_882cedd8-b1df-445a-b8cf-e9bdb1341b44.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CLINDAMYCIN HYDROCHLORIDEACTIVE INGREDIENTT20OQ1YN1WCLINDACURE (CLINAMYCIN HYDROCHLORIDE) LIQUID [VEDCO]2
CLINDAMYCINACTIVE MOIETY3U02EL437CCLINDACURE (CLINAMYCIN HYDROCHLORIDE) LIQUID [VEDCO]2