Precedex
Brand Name: Precedex
Generic Name: Dexmedetomidine (as hydrochloride)
Active
Registration Number
DR-XY32202
Dosage Form
Concentrate For Intravenous Infusion
Issuance Date
July 1, 2024
Expiry Date
August 21, 2029
Product Information
Philippine FDA product specifications and classification details
Product Specifications
Dosage Strength100 mcg/mL (200 mcg/2 mL)
Packaging2 mL USP Type I clear and colorless glass vial (Box of 5's)
Classification
C
Classification
Prescription Drug (RX)
P
Pharmacologic
Hypnotic / Sedative
A
Application
Renewal
Philippine FDA Classification
Active Ingredients (1)
Complete list of active ingredients in this pharmaceutical product.
Dexmedetomidine (as hydrochloride)Active
Monograph: Buccal Dexmedetomidine (Reconnect Labs)