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Latrela - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Latrela

Approved

STANDARD

Latrela

Takeda Pharmaceutical Company Limited (Osaka Plant)🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 5d7fc7befd668d9d
Company: Takeda Pharmaceutical Company Limited (Osaka Plant)
Type: Standard

Approval Details

Approval Id: 5d7fc7befd668d9d
Drug Approval Philippines Name: Latrela
Product Name: Latrela
Registration Number: DR-XY47110
Brand Name: Latrela
Generic Name: Trelagliptin (as succinate)
Dosage Form: Film-Coated Tablet
Dosage Strength: 100mg
Manufacturer: Takeda Pharmaceutical Company Limited (Osaka Plant)
Importer: Takeda Healthcare Philippines, Inc.
Issuance Date: 27 November 2020
Expiry Date: 27 November 2025
Pharmacologic Category: Anti-Diabetes
Classification: Prescription Drug (Rx)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

5d7fc7befd668d9d

Type

Standard

Back to Philippines FDA Approvals