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PROLIDE - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/PROLIDE

Approved

STANDARD

PROLIDE

Celon Laboratories Limited🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: a4bfff57ae5ba617
Company: Celon Laboratories Limited
Type: Standard

Approval Details

Approval Id: a4bfff57ae5ba617
Drug Approval Philippines Name: PROLIDE
Product Name: PROLIDE
Registration Number: DRP-7243
Brand Name: PROLIDE
Generic Name: Leuprorelin Acetate
Dosage Form: Lyophilized Powder for Injection
Dosage Strength: 11.25 mg
Manufacturer: Celon Laboratories Limited
Importer: I.E. MEDICA INC.
Distributor: I.E. MEDICA INC.
Issuance Date: 24 June 2022
Expiry Date: 21 June 2027
Pharmacologic Category: Antineoplastic
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

a4bfff57ae5ba617

Type

Standard

Back to Philippines FDA Approvals