FDA.reportPublic FDA data

NDC 23243-2320-6 - PROHIBIT Soluble Drench Powder

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
23243-2320
Requested NDC
23243-2320-6
Package NDCs from labels
23243-2320-5, 23243-2320-6
Manufacturer
Huvepharma, Inc | Huvepharma EOOD
Effective date
2026-07-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PROHIBIT Soluble Drench Powder - Huvepharma, Inc | Huvepharma EOODHuvepharma, Inc | Huvepharma EOOD2026-07-07OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
23243-2320-5PROHIBITSoluble Drench Powder52 g in 1 PACKETPOWDER, FOR SOLUTION523
23243-2320-6PROHIBITSoluble Drench Powder605 g in 1 JUGPOWDER, FOR SOLUTION6053

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
23243-2320PROHIBIT SOLUBLE DRENCH POWDER (LEVAMISOLE HYDROCHLORIDE) POWDER, FOR SOLUTION [HUVEPHARMA, INC]32 package rows20240529_baf0da35-573e-4abb-bdef-18870d5f5f72.zip

Reported adverse events (FAERS/openFDA)#

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