NDC 58829-293-08 - PRIVERMECTIN DRENCH FOR SHEEP

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
58829-293
Requested NDC
58829-293-08
Package NDCs from labels
58829-293-08, 58829-293-32
Manufacturer
FIRST PRIORITY INCORPORATED
Effective date
2024-09-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
PRIVERMECTIN DRENCH FOR SHEEP - FIRST PRIORITY INCORPORATEDFIRST PRIORITY INCORPORATED2024-09-03OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58829-293-08PRIVERMECTIN DRENCH FOR SHEEP240 mL in 1 JUGLIQUID24015
58829-293-08PRIVERMECTIN DRENCH FOR SHEEP6 in 1 CASELIQUID615
58829-293-32PRIVERMECTIN DRENCH FOR SHEEP960 mL in 1 JUGLIQUID96015
58829-293-32PRIVERMECTIN DRENCH FOR SHEEP4 in 1 CASELIQUID415

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58829-293PRIVERMECTIN DRENCH FOR SHEEP (IVERMECTIN) LIQUID [FIRST PRIORITY INCORPORATED]154 package rows20240905_826300ef-ec81-41c8-8184-ad74fe2ab11d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
IVERMECTINACTIVE INGREDIENT8883YP2R6DPRIVERMECTIN DRENCH FOR SHEEP (IVERMECTIN) LIQUID [FIRST PRIORITY INCORPORATED]7
IVERMECTINACTIVE MOIETY8883YP2R6DPRIVERMECTIN DRENCH FOR SHEEP (IVERMECTIN) LIQUID [FIRST PRIORITY INCORPORATED]7

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 · 34 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SOOLANTRAIVERMECTINGalderma Laboratories, L.P.b1d5b166-ab06-4ab5-b0c6-31126238118a2024-10-24Adverse reactionsExact identifier
unii: 8883YP2R6D
STROMECTOLIVERMECTINMerck Sharp & Dohme LLC681888c9-af79-4b7d-ae80-c3f4f6f1effd2024-09-20Warnings, Adverse reactionsExact identifier
unii: 8883YP2R6D
ivermectinIVERMECTINEPIC PHARMA LLCc8005642-3bf0-41b9-8a53-8b933c68c0732024-08-28Warnings, Adverse reactionsExact identifier
unii: 8883YP2R6D
IvermectinIVERMECTINRite Aid Corporation3a2eb7f3-b72b-435c-a609-ce7050cccff42024-08-12WarningsExact identifier
unii: 8883YP2R6D
IvermectinIVERMECTINNuCare Pharmaceuticals,Inc.ad6539f2-94de-1bc5-e053-2a95a90a4cf22024-07-17Warnings, Adverse reactionsExact identifier
unii: 8883YP2R6D
SkliceIVERMECTINAzurity Pharmaceuticals7579bdfe-a538-4bff-b7c7-df2c4b6f13db2024-07-11WarningsExact identifier
unii: 8883YP2R6D
IvermectinIVERMECTINBryant Ranch Prepack75973e89-a03f-48dd-8fe8-8eafc1938d092024-04-30Adverse reactionsExact identifier
unii: 8883YP2R6D
IvermectinIVERMECTINPadagis Israel Pharmaceuticals Ltd1d3e7aea-02a4-46b1-8a14-0324e4777cb42024-03-31Adverse reactionsExact identifier
unii: 8883YP2R6D
ivermectinIVERMECTINViona Pharmaceuticals Inc6b4a7400-d34c-4947-90e6-340f7087a7022024-03-27Adverse reactionsExact identifier
unii: 8883YP2R6D
IvermectinIVERMECTINBryant Ranch Prepack81193a2d-dc0a-4ce5-a5c1-6dfd3195c4bc2023-10-30Adverse reactionsExact identifier
unii: 8883YP2R6D
IvermectinIVERMECTINAsclemed USA, Inc.014e33e7-c07d-4feb-a2cf-7cd160b1facd2023-10-05Warnings, Adverse reactionsExact identifier
unii: 8883YP2R6D
IVERMECTINIVERMECTINMayne Pharma Inc.39fbf2b3-cd2f-4e04-99c4-ca4390fae2bd2023-08-29Adverse reactionsExact identifier
unii: 8883YP2R6D
ivermectinIVERMECTINZydus Lifesciences Limited22e85f9a-0805-47f2-8709-aa6514511b042023-06-07Exact identifier
unii: 8883YP2R6D
IvermectinIVERMECTINWalgreen Companyb8e1d919-ba66-4dc0-b0fc-cfb3a229dad92022-01-04WarningsExact identifier
unii: 8883YP2R6D

Reported adverse events (FAERS/openFDA)#

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