NDC 86012-3003 - Integrity Pre-Post Part A

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
86012-3003
Package NDCs from labels
86012-3003-1, 86012-3003-2, 86012-3003-3, 86012-3003-4
Manufacturer
Premier Select Sires
Effective date
2022-11-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Integrity Pre-Post Part A - Premier Select SiresPremier Select Sires2022-11-21OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86012-3003-1Integrity Pre-Post Part A19 kg in 1 CONTAINERSOLUTION191
86012-3003-2Integrity Pre-Post Part A57 kg in 1 DRUMSOLUTION571
86012-3003-3Integrity Pre-Post Part A208 kg in 1 DRUMSOLUTION2081
86012-3003-4Integrity Pre-Post Part A1041 kg in 1 CONTAINERSOLUTION10411

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86012-3003INTEGRITY PRE-POST PART A (LACTIC ACID) SOLUTION [PREMIER SELECT SIRES]14 package rows20221123_ea163dff-3aed-4c51-a032-855bc49ca293.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 2 of 2 · 21 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Glucose Control T015SYZYGIUM JAMBOLANUM, GLANDULA SUPRARENALIS SUIS, HYDRASTIS CANADENSIS, HYPOPHYSIS SUIS, PANCREAS SUIS, PHASEOLUS, ACETICUM ACIDUM, LACTICUM ACIDUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, URANIUM NITRICUMGuangzhou Renuma Medical Systems Co., Ltd3fd02c0a-5cf1-4f35-86d0-d5d09e63f39b2017-10-26WarningsExact identifier
unii: 33X04XA5AT

Reported adverse events (FAERS/openFDA)#

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