Testosterone Cypionate
Testosterone Cypionate Injection, USP CIII
Approved
Approval ID
58ff6e0d-cc0a-4455-8254-d883d26a3b6d
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 6, 2019
Manufacturers
FDA
Wilshire Pharmaceuticals
DUNS: 078657245
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
testosterone cypionate
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52536-625
Application NumberANDA206368
Product Classification
M
Marketing Category
C73584
G
Generic Name
testosterone cypionate
Product Specifications
Route of AdministrationINTRAMUSCULAR
Effective DateMay 10, 2019
FDA Product Classification
INGREDIENTS (4)
testosterone cypionateActive
Quantity: 200 mg in 1 mL
Code: M0XW1UBI14
Classification: ACTIB
benzyl benzoateInactive
Code: N863NB338G
Classification: IACT
benzyl alcoholInactive
Code: LKG8494WBH
Classification: IACT
cottonseed oilInactive
Code: H3E878020N
Classification: IACT