Luprodex
Brand Name: Luprodex
Generic Name: Leuprorelin acetate
Active
Registration Number
DRP-7757
Dosage Form
Lyophilized Powder for Injection (IM/SC)
Issuance Date
June 20, 2022
Expiry Date
June 20, 2027
Product Information
Philippine FDA product specifications and classification details
Product Specifications
Dosage Strength3.75 mg
PackagingUSP Type I Clear, Colorless Glass Vial with orange
aluminium flip-off seal with USP Type I Clear Glass Ampoule containing 2 mL of diluent, 2 22G needles, 3 mL syringe and 2 alcohol swabs in a transparent PVC plastic tray in a box
Classification
C
Classification
Prescription Drug (RX)
P
Pharmacologic
Gonadotropin Releasing Hormone (GnRH) Analogue
A
Application
Initial (Variation)
Philippine FDA Classification
Active Ingredients (1)
Complete list of active ingredients in this pharmaceutical product.
Leuprorelin acetateActive
Monograph: Leuprolide