Testo-100
Testo-100
Approved
Approval ID
593ebdf5-54c6-7fae-e053-2991aa0a8e4a
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Nov 4, 2023
Manufacturers
FDA
Advanced Pharmaceutical Technology, Inc.
DUNS: 023237884
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Testosterone,USP
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code57377-100
Product Classification
G
Generic Name
Testosterone,USP
Product Specifications
Route of AdministrationSUBCUTANEOUS
Effective DateNovember 4, 2023
FDA Product Classification
INGREDIENTS (3)
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
TESTOSTERONEActive
Quantity: 100 mg in 1 1
Code: 3XMK78S47O
Classification: ACTIB