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Acteinsaph-600 - Philippines FDA Drug Approval Details

Approvals/Philippines FDA/Acteinsaph-600

Approved

STANDARD

Acteinsaph-600

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

Approval Date: Jul 14, 2025
Approval ID: 8f6275bfd63fc180
Company: Sapphire Lifesciences Pvt. Ltd.
Type: Standard

Approval Details

Approval Id: 8f6275bfd63fc180
Drug Approval Philippines Name: Acteinsaph-600
Product Name: Acteinsaph-600
Registration Number: DRP-10618
Brand Name: Acteinsaph-600
Generic Name: Acetylcysteine
Dosage Form: Effervescent tablet
Dosage Strength: 600 mg
Manufacturer: Sapphire Lifesciences Pvt. Ltd.
Importer: Nelpa Lifesciences, Inc.
Distributor: Nelpa Lifesciences, Inc.
Issuance Date: 25 October 2021
Expiry Date: 25 October 2026
Pharmacologic Category: Mucolytic
Classification: Prescription Drug (RX)

Active Ingredients

Approved

Quick Info

Agency

Philippines FDA

Country

🇵🇭

Approval Date

Jul 14, 2025

Approval ID

8f6275bfd63fc180

Type

Standard

Back to Philippines FDA Approvals