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Shelogel - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Shelogel

Approved

STANDARD

Shelogel

Scheele Laboratories Phils., Inc🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 69a3cfc1642fccf9
Company: Scheele Laboratories Phils., Inc
Type: Standard

Approval Details

Approval Id: 69a3cfc1642fccf9
Drug Approval Philippines Name: Shelogel
Product Name: Shelogel
Registration Number: DRP-10215
Brand Name: Shelogel
Generic Name: Aluminum Hydroxide + Magnesium
Dosage Form: Tablet
Dosage Strength: 200 mg/100 mg
Manufacturer: Scheele Laboratories Phils., Inc
Issuance Date: 27 February 2024
Expiry Date: 02 June 2026
Pharmacologic Category: Antacid
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

69a3cfc1642fccf9

Type

Standard

Back to Philippines FDA Approvals