Home NDC 62935-154 NDC 62935-154 - Fensolvi 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 62935-154
Package NDCs from labels 62935-154-50
Manufacturer TOLMAR Inc.
Effective date 2022-04-28
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Fensolvi - TOLMAR Inc. TOLMAR Inc. 2022-04-28 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 62935-154-50 Fensolvi 0.375 mL in 1 SYRINGE INJECTION, SUSPENSION, EXTENDED 0.375 mL 45 mg in 0.375mL 17
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 62935-154 FENSOLVI (LEUPROLIDE ACETATE) KIT [TOLMAR INC.] 17 Unmatched 20231206_dfb6e01c-f138-471d-bf5b-2be38247e3f0.zip