FDA.reportPublic FDA data

NDC 86032-027 - Cloprostenol Sodium

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
86032-027
Package NDCs from labels
86032-027-01
Manufacturer
Evereen Shanghai Biotechnology Ltd. | TIEN (Tianjin) Pharmaceutical Co. Ltd
Effective date
2024-08-20
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Cloprostenol SodiumEvereen Shanghai Biotechnology Ltd. | TIEN (Tianjin) Pharmaceutical Co. Ltd2024-08-20BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
86032-027-01Cloprostenol Sodium5 g in 1 BAGPOWDER51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
86032-027CLOPROSTENOL SODIUM POWDER [EVEREEN SHANGHAI BIOTECHNOLOGY LTD.]11 package rows20240821_6d4fa371-7879-4010-b47b-101c9a644ff5.zip

Reported adverse events (FAERS/openFDA)#

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