NDC 51429-343 - Pennox 343

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
51429-343
Package NDCs from labels
51429-343-02
Manufacturer
Pharmgate Animal Health | Pharmgate Inc.
Effective date
2026-09-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Pennox 343 ® (oxytetracycline HCl) Soluble PowderPharmgate Animal Health | Pharmgate Inc.2026-09-11PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51429-343-02Pennox 343677.6 g in 1 POUCHPOWDER677.69

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51429-343PENNOX 343 (OXYTETRACYCLINE HYDROCHLORIDE) POWDER [PHARMGATE ANIMAL HEALTH]91 package rows20221021_eb83ae41-c32b-47dd-8459-506b33ccb6ba.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Oxytetracycline HydrochlorideACTIVE INGREDIENT4U7K4N52ZMPENNOX 343 (OXYTETRACYCLINE HYDROCHLORIDE) POWDER [PHARMGATE ANIMAL HEALTH]4
Oxytetracycline AnhydrousACTIVE MOIETYSLF0D9077SPENNOX 343 (OXYTETRACYCLINE HYDROCHLORIDE) POWDER [PHARMGATE ANIMAL HEALTH]4

Reported adverse events (FAERS/openFDA)#

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