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Atomoxetine (As Hydrochloride) - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Atomoxetine (As Hydrochloride)

Approved

STANDARD

Atomoxetine (As Hydrochloride)

Lilly Del Caribe Inc.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: c6703f85304e29af
Company: Lilly Del Caribe Inc.
Type: Standard

Approval Details

Approval Id: c6703f85304e29af
Drug Approval Philippines Name: Atomoxetine (As Hydrochloride)
Product Name: Atomoxetine (As Hydrochloride)
Registration Number: DR-XY44710
Brand Name: Atomoxetine (As Hydrochloride)
Generic Name: Strattera
Dosage Form: Capsule
Dosage Strength: 25 mg
Manufacturer: Lilly Del Caribe Inc.
Importer: Zuellig Pharma Corporation
Distributor: Zuellig Pharma Corporation
Issuance Date: 24 July 2020
Expiry Date: 10 July 2025
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

c6703f85304e29af

Type

Standard

Back to Philippines FDA Approvals