Fonkomustin
Brand Name: Fonkomustin
Generic Name: Bendamustine Hydrochloride (as monohydrate)
Active
Registration Number
DRP-12247
Dosage Form
Lyophilized Powder For Injection (IV)
Issuance Date
July 1, 2022
Expiry Date
July 1, 2027
Product Information
Philippine FDA product specifications and classification details
Product Specifications
Dosage Strength100 mg
PackagingUSP Type I amber glass vial with grey bromo butyl
rubber stopper and blue flip off seal x 20 mL (Box of 1’s)
Classification
C
Classification
Prescription Drug (RX)
P
Pharmacologic
Antineoplastic (Nitrogen Mustard Analogue)
A
Application
Initial
Philippine FDA Classification
Active Ingredients (1)
Complete list of active ingredients in this pharmaceutical product.
Bendamustine Hydrochloride (as monohydrate)Active
Monograph: bendamustine hydrochloride (as monohydrate)