NDC 23243-6807 - Bio-Cox Type A Medicated Article

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
23243-6807
Package NDCs from labels
23243-6807-5
Manufacturer
Huvepharma, Inc. | Huvepharma EOOD | Huvepharma, Inc - Van Buren
Effective date
2023-09-13
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SALINOMYCIN - Huvepharma, Inc. | Huvepharma EOOD | Huvepharma, Inc - Van BurenHuvepharma, Inc. | Huvepharma EOOD | Huvepharma, Inc - Van Buren2023-09-13OTC TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-6807-5Bio-Cox Type A Medicated Article22.68 kg in 1 BAGPOWDER22.686

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-6807BIO-COX TYPE A MEDICATED ARTICLE (SALINOMYCIN SODIUM) POWDER [HUVEPHARMA, INC.]61 package rows20230926_7f47cb02-eb4b-4ff9-9d41-4a22a60cca94.zip

Reported adverse events (FAERS/openFDA)#

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