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Levomax - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Levomax

Approved

STANDARD

Levomax

The Acme Laboratories Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 9d167f8007db2313
Company: The Acme Laboratories Ltd.
Type: Standard

Approval Details

Approval Id: 9d167f8007db2313
Drug Approval Philippines Name: Levomax
Product Name: Levomax
Registration Number: DRP-1726
Brand Name: Levomax
Generic Name: Levofloxacin (as hemihydrate)
Dosage Form: Film Coated Tablet
Dosage Strength: 500 mg
Manufacturer: The Acme Laboratories Ltd.
Importer: Euro Generics International Phils., Inc.
Distributor: Euro Generics International Phils., Inc.
Company Detail Path: /organization/153a2a520aa7581f/the-acme-laboratories-ltd
Issuance Date: 31 October 2023
Expiry Date: 19 May 2029
Pharmacologic Category: Antibacterial (Third Generation Quinolone)
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

9d167f8007db2313

Type

Standard

Back to Philippines FDA Approvals