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Nagelin (Reformulated) - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Nagelin (Reformulated)

Approved

STANDARD

Nagelin (Reformulated)

La Croesus Pharma, Inc.🇵🇭 Food and Drug Administration - Philippines

Approval Date: Jul 14, 2025
Approval ID: 70786592a9f8254d
Company: La Croesus Pharma, Inc.
Type: Standard

Approval Details

Approval Id: 70786592a9f8254d
Drug Approval Philippines Name: Nagelin (Reformulated)
Product Name: Nagelin (Reformulated)
Registration Number: DR-XY42858
Brand Name: Nagelin (Reformulated)
Generic Name: Paracetamol + Phenylephrine HCl + Chlorpheniramine Maleate
Dosage Form: Capsule
Dosage Strength: 325 mg/25mg/2mg
Manufacturer: La Croesus Pharma, Inc.
Trader: IAE Pharmaceuticals Corporation
Issuance Date: 24 October 2023
Expiry Date: 23 October 2028
Pharmacologic Category: Analgesic/Antipyretic/Decongestant/Antihistamine
Classification: Over-The-Counter (OTC)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

70786592a9f8254d

Type

Standard

Back to Philippines FDA Approvals