Testozole
Testozole 60mg/4mg
Approved
Approval ID
d3c42530-07dd-8a7d-e053-2a95a90ab2b6
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 27, 2022
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 Code57377-060
Product Classification
G
Generic Name
Testosterone,USP
Product Specifications
Route of AdministrationSUBCUTANEOUS
Effective DateMay 27, 2022
FDA Product Classification
INGREDIENTS (4)
STEARIC ACIDInactive
Code: 4ELV7Z65AP
Classification: IACT
TESTOSTERONEActive
Quantity: 60 mg in 1 1
Code: 3XMK78S47O
Classification: ACTIB
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
ANASTROZOLEActive
Quantity: 4 mg in 1 1
Code: 2Z07MYW1AZ
Classification: ACTIB