Nicardilex
Brand Name: Nicardilex
Generic Name: Nicardipine hydrochloride
Active
Registration Number
DRP-15060
Dosage Form
Solution for Injection (I.V.)
Issuance Date
April 1, 2024
Expiry Date
April 1, 2029
Product Information
Philippine FDA product specifications and classification details
Product Specifications
Dosage Strength1 mg/mL (20 mg/20 mL)
Packaging20 mL-net content USP Type I amber glass vial with grey
glass vial butyl rubber stopper and aluminum seal with green plastic flip-off cap (Box of 1's)
Classification
C
Classification
Prescription (Rx) Drug
P
Pharmacologic
Calcium Channel Blocker (Dihydropyridine Derivative)
A
Application
Initial
Philippine FDA Classification
Active Ingredients (1)
Complete list of active ingredients in this pharmaceutical product.
Nicardipine hydrochlorideActive
Monograph: Nicardipine