FDA.reportPublic FDA data

NDC 51311-444 - Suprelorin F

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
51311-444
Package NDCs from labels
51311-444-05, 51311-444-02
Manufacturer
Virbac AH, Inc. | Polypeptide Laboratories Inc | Peptech Animal Health PTY Limited
Effective date
2022-01-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Suprelorin ® F (DESLORELIN ACETATE) 4.7 mg ImplantVirbac AH, Inc. | Polypeptide Laboratories Inc | Peptech Animal Health PTY Limited2022-01-07PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51311-444-02Suprelorin F1 in 1 SYRINGEIMPLANT13
51311-444-02Suprelorin F2 in 1 CARTONIMPLANT23
51311-444-05Suprelorin F5 in 1 CARTONIMPLANT53
51311-444-05Suprelorin F1 in 1 SYRINGEIMPLANT13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51311-444SUPRELORIN F (DESLORELIN ACETATE) IMPLANT [VIRBAC AH, INC.]34 package rows20220108_aa5776dc-277e-4a5e-885f-6e3f05c8404b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
deslorelin acetateACTIVE INGREDIENT679007NR5CSUPRELORIN F (DESLORELIN ACETATE) IMPLANT [VIRBAC AH, INC.]1
deslorelinACTIVE MOIETYTKG3I66TVESUPRELORIN F (DESLORELIN ACETATE) IMPLANT [VIRBAC AH, INC.]1

Reported adverse events (FAERS/openFDA)#

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