Home NDC 57377-100 NDC 57377-100 - Testo-100 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 57377-100
Package NDCs from labels 57377-100-01
Manufacturer Advanced Pharmaceutical Technology, Inc.
Effective date 2024-09-05
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Testo-100 Advanced Pharmaceutical Technology, Inc. 2024-09-05 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 57377-100-01 Testo-100 10 in 1 AMPULE PELLET, IMPLANTABLE 10 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 57377-100 TESTO-100 (TESTOSTERONE,USP) PELLET, IMPLANTABLE [ADVANCED PHARMACEUTICAL TECHNOLOGY, INC.] 10 1 package rows 20240925_593ebdf5-54c6-7fae-e053-2991aa0a8e4a.zip