FDA.reportPublic FDA data

NDC 23243-2350-1 - Tylovet 100 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
23243-2350
Requested NDC
23243-2350-1
Package NDCs from labels
23243-2350-1
Manufacturer
Huvepharma, Inc. | Huvepharma EOOD
Effective date
2023-04-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tylovet 100 Type A Medicated Article - Huvepharma, Inc. | Huvepharma EOODHuvepharma, Inc. | Huvepharma EOOD2023-04-11VFD TYPE A MEDICATED ARTICLE ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-2350-1Tylovet 100 Type A Medicated Article22.68 kg in 1 BAGPOWDER22.688

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-2350TYLOVET 100 TYPE A MEDICATED ARTICLE (TYLOSIN PHOSPHATE) POWDER [HUVEPHARMA, INC.]81 package rows20230418_dac46d7b-d852-42ca-822b-32ba0faf5038.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
TYLOSIN PHOSPHATEACTIVE INGREDIENTNR75X12AFFTYLOVET 100 (TYLOSIN PHOSPHATE) POWDER [HUVEPHARMA, INC.]3
TYLOSINACTIVE MOIETYYEF4JXN031TYLOVET 100 (TYLOSIN PHOSPHATE) POWDER [HUVEPHARMA, INC.]3

Reported adverse events (FAERS/openFDA)#

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