MedPath

Omee

Brand Name: Omee

Generic Name: Omeprazole (as Sodium)

Active
Registration Number

DRP-5882-04

Dosage Form

Lyophilized Powder For IV Injection/Infusion

Issuance Date

September 28, 2022

Expiry Date

December 9, 2027

Product Information

Philippine FDA product specifications and classification details

Product Specifications

Dosage Strength40 mg
Packaging10 mL USP Type 1 Amber Glass Vial + 10 mL USP Type 1 Clear and Colorless Glass Ampoule containing Sterile Water for Injection (as diluent) (Box of 1's)

Classification

C
Classification
Prescription Drug (RX)
P
Pharmacologic
Proton Pump Inhibitor
A
Application
Automatic Renewal
Philippine FDA Classification

Active Ingredients (1)

Complete list of active ingredients in this pharmaceutical product.

Omeprazole (as Sodium)Active
Monograph: omeprazole (as sodium)

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

Product

Company

Legal

© 2025 MedPath, Inc. All rights reserved.

MedPath - Medical Intelligence Platform