NDC 13985-036 - PenOne Pro

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
13985-036
Package NDCs from labels
13985-036-02, 13985-036-04, 13985-036-05
Manufacturer
MWI Veterinary Supply Co | Norbrook Laboratories Limited
Effective date
2023-06-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PenOne Pro - MWI Veterinary Supply Co | Norbrook Laboratories LimitedMWI Veterinary Supply Co | Norbrook Laboratories Limited2023-06-01PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
13985-036-02PenOne Pro100 mL in 1 VIAL, GLASSINJECTION, SUSPENSION1004
13985-036-04PenOne Pro250 mL in 1 VIAL, GLASSINJECTION, SUSPENSION2504
13985-036-05PenOne Pro500 mL in 1 VIAL, GLASSINJECTION, SUSPENSION5004

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
13985-036PENONE PRO (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [MWI VETERINARY SUPPLY CO]43 package rows20230609_4049a09f-422f-4220-99ef-8dd6b846945b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
penicillin G procaineACTIVE INGREDIENT17R794ESYNPENONE PRO (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [MWI/VETONE]1
penicillin GACTIVE MOIETYQ42T66VG0CPENONE PRO (PENICILLIN G PROCAINE) INJECTION, SUSPENSION [MWI/VETONE]1

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 26 of 26 · 504 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ReHydrationADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI PHOSPHORICUM, NATRUM MURIATICUM, SARSAPARILLA, SILICEA, TARAXACUM OFFICINALE, THYROIDINUM (BOVINE)Energetix Corp9883c502-9782-451e-9eec-c54d7b054f312017-01-31WarningsExact identifier
unii: CI71S98N1Z
CerebroforceCAPSICUM ANNUUM, GINKGO BILOBA, GELSEMIUM SEMPERVIRENS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, PHOSPHORUS, ARSENICUM ALBUMBioActive Nutritional, Incf998ed3f-56a5-4497-be5b-9a819fe8be692016-07-13WarningsExact identifier
unii: CI71S98N1Z
Sterile WaterWATERBaxter Healthcare Company210dc9ab-d6ca-4552-ac19-1be17792d2902016-05-31Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
TIS-U-SOLSODIUM CHLORIDE, POTASSIUM CHLORIDE, MAGNESIUM SULFATE, SODIUM PHOSPHATE, AND POTASSIUM PHOSPHATEBaxter Healthcare Corporation9da4121f-d62d-4da4-8dfb-0494da16015f2014-02-21Exact identifier
unii: 4J9FJ0HL51

Reported adverse events (FAERS/openFDA)#

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