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Anemifer - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Anemifer

Approved

STANDARD

Anemifer

AM-Europharma Corporation🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: fb91026e726ab02f
Company: AM-Europharma Corporation
Type: Standard

Approval Details

Approval Id: fb91026e726ab02f
Drug Approval Philippines Name: Anemifer
Product Name: Anemifer
Registration Number: DRP-7846
Brand Name: Anemifer
Generic Name: Ferrous Sulfate Heptahydrate
Dosage Form: Syrup
Dosage Strength: 150 mg / 5 mL (equivalent to 30 mg elemental iron)
Manufacturer: AM-Europharma Corporation
Issuance Date: 26 March 2022
Expiry Date: 30 August 2027
Pharmacologic Category: Anti-anemic
Classification: Over-The-Counter (OTC)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

fb91026e726ab02f

Type

Standard

Back to Philippines FDA Approvals