Gemget 200
Brand Name: Gemget 200
Generic Name: Gemcitabine (as hydrochloride)
Active
Registration Number
DRP-16570
Dosage Form
Lyophilized Powder for Injection (IV)
Issuance Date
April 29, 2025
Expiry Date
April 29, 2030
Product Information
Philippine FDA product specifications and classification details
Product Specifications
Dosage Strength200 mg
Packaging10 mL-capacity, type I clear glass vial with rubber stopper and aluminum green flip-off seal (Box of 1's)
Classification
C
Classification
Prescription (Rx) Drug
P
Pharmacologic
Antineoplastic Agent
A
Application
Initial
Philippine FDA Classification
Active Ingredients (1)
Complete list of active ingredients in this pharmaceutical product.
Gemcitabine (as hydrochloride)Active
Monograph: HPMA-gemcitabine