Home NDC 10702-366 NDC 10702-366 - 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 10702-366
Package NDCs from labels 10702-366-03
Manufacturer KVK-Tech, Inc.
Effective date 2025-11-14
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Carmustine - KVK-Tech, Inc. KVK-Tech, Inc. 2025-11-14 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 10702-366-03 Carmustine 30 mL in 1 VIAL, SINGLE-DOSE INJECTION, POWDER, LYOPHILIZED, 30 mL 100 mg in 30mL 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 10702-366 CARMUSTINE KIT [KVK-TECH, INC.] 1 Unmatched 20240307_11c3fad8-65ef-39a7-e063-6294a90a73e1.zip