FDA.reportPublic FDA data

NDC 70121-1668 - carmustine

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
70121-1668
Package NDCs from labels
70121-1668-1
Manufacturer
Amneal Pharmaceuticals LLC
Effective date
2023-06-03
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
carmustine - Amneal Pharmaceuticals LLCAmneal Pharmaceuticals LLC2023-06-03HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70121-1668-1carmustine30 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, LYOPHILIZED,30 mL100 mg in 30mL8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70121-1668CARMUSTINE KIT [AMNEAL PHARMACEUTICALS LLC]8Unmatched20231104_2df937ad-a458-4030-bb7b-4468baa3685e.zip