NDC 50378-016-02 - Tricaine methanesulfonate

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
50378-016
Requested NDC
50378-016-02
Package NDCs from labels
50378-016-01, 50378-016-02, 50378-016-03
Manufacturer
Western Chemical Inc.
Effective date
2023-05-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Tricaine methanesulfonateWestern Chemical Inc.2023-05-31OTC ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50378-016-01Tricaine methanesulfonate100 g in 1 BOTTLE, PLASTICPOWDER, FOR SOLUTION1001
50378-016-02Tricaine methanesulfonate1000 g in 1 BOTTLE, PLASTICPOWDER, FOR SOLUTION10001
50378-016-03Tricaine methanesulfonate20000 g in 1 DRUMPOWDER, FOR SOLUTION200001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50378-016TRICAINE METHANESULFONATE POWDER, FOR SOLUTION [WESTERN CHEMICAL INC.]13 package rows20230602_754a0b57-c07c-491b-89e1-86a0c631a830.zip

Reported adverse events (FAERS/openFDA)#

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