FDA.reportPublic FDA data

NDC 86117-042 - PHENYLPROPANOLAMINE HYDROCHLORIDE

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
86117-042
Package NDCs from labels
86117-042-05, 86117-042-09
Manufacturer
ZYVET ANIMAL HEALTH INC.
Effective date
2026-10-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Phenylpropanolamine Hydrochloride Chewable TabletsZYVET ANIMAL HEALTH INC.2026-10-05PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86117-042-05PHENYLPROPANOLAMINE HYDROCHLORIDE60 in 1 BOTTLETABLET, CHEWABLE602
86117-042-09PHENYLPROPANOLAMINE HYDROCHLORIDE180 in 1 BOTTLETABLET, CHEWABLE1802

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86117-042PHENYLPROPANOLAMINE HYDROCHLORIDE TABLET, CHEWABLE [ZYVET ANIMAL HEALTH INC.]12 package rows20241008_a2843a87-265e-4d47-a89b-bee88107b0a6.zip

Reported adverse events (FAERS/openFDA)#

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