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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