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LERIF - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/LERIF

Approved

STANDARD

LERIF

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

Approval Date: Jul 14, 2025
Approval ID: 030c9ee2386ded13
Company: LifeSquare Laboratories, Inc.
Type: Standard

Approval Details

Approval Id: 030c9ee2386ded13
Drug Approval Philippines Name: LERIF
Product Name: LERIF
Registration Number: DRP-5185-08
Brand Name: LERIF
Generic Name: CETIRIZINE (as dihydrochloride)
Dosage Form: Tablet
Dosage Strength: 10 mg
Manufacturer: LifeSquare Laboratories, Inc.
Distributor: Alman Pharmaceuticals, Inc
Issuance Date: 26 March 2024
Expiry Date: 03 March 2029
Pharmacologic Category: ANTIHISTAMINE
Classification: Prescription Drug (Rx)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

030c9ee2386ded13

Type

Standard

Back to Philippines FDA Approvals