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Moxeth-250 - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Moxeth-250

Approved

STANDARD

Moxeth-250

Sapphire Lifesciences Pvt. Ltd.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 8b34d12f529f01d6
Company: Sapphire Lifesciences Pvt. Ltd.
Type: Standard

Approval Details

Approval Id: 8b34d12f529f01d6
Drug Approval Philippines Name: Moxeth-250
Product Name: Moxeth-250
Registration Number: DRP-4909-01
Brand Name: Moxeth-250
Generic Name: Amoxicillin (as Trihydrate)
Dosage Form: Powder For Oral Suspension
Dosage Strength: 250 mg/5 mL
Manufacturer: Sapphire Lifesciences Pvt. Ltd.
Importer: Nelpa Lifesciences, Inc.
Distributor: 777 Red Pharma Inc.
Issuance Date: 24 January 2024
Expiry Date: 17 December 2028
Pharmacologic Category: Antibacterial (Penicillin)
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

8b34d12f529f01d6

Type

Standard

Back to Philippines FDA Approvals