Skip to main content

Clinical TrialsSearch 1M+ trials from global registries Drug IntelligenceFollow pipelines from discovery to approval

Global ApprovalsTrack regulatory decisions across 12+ agencies

US FDA Drugs EU EMA Drugs Singapore HSA Drugs China NMPA Drugs Australia TGA Drugs Canada HC Drugs Spain CIMA-AEMPS Drugs UK EMC Drugs Saudi SFDA Drugs Malaysia NPRA Drugs Philippines FDA Drugs Kenya PPB Drugs

AI-Powered ResearchDiscover powerful insights with advanced AI analysis tools for clinical trials.Learn more →Premium AccessGet unlimited access to our comprehensive pharmaceutical database and analytics.Subscribe →

Organizations News Research

Data Sources:ClinicalTrials.govEU CTRFDAEMANMPATGAHealth CanadaWHO ICTRP

Search trials. Track pipelines. Understand approvals. With AI-powered intelligence for clinical research.

Product

Clinical Trials
Drug Intelligence
Global Approvals
AI Research
Pricing

Resources

FAQ
Search

Company

News
About
Contact

Legal

Privacy Policy
Terms of Service

Disclaimer: This website provides information retrieval and data analysis services. The content does not constitute medical advice. Eligibility assessments are for reference only and should not replace consultation with qualified healthcare professionals. Data is sourced from public registries and regulatory agencies; MedPath does not guarantee completeness or accuracy. Always verify information with primary sources.

© 2026 MedPath. All rights reserved.

We value your privacy

We use cookies to analyze site traffic and improve your experience. See our Privacy Policy.

AQUIPTA TABLET 60MG - HSA Drug Approval Details

Approvals/HSA/AQUIPTA TABLET 60MG

Approved

THERAPEUTIC

AQUIPTA TABLET 60MG

Forest Laboratories Ireland, Limited🇸🇬 Health Sciences Authority

Approval Date: Nov 29, 2024
Approval ID: ad008fab522859fe
Company: Forest Laboratories Ireland, Limited
Type: Therapeutic

Approval Details

Approval Id: ad008fab522859fe
Drug Name: AQUIPTA TABLET 60MG
Product Name: AQUIPTA TABLET 60MG
Approval Number: SIN17146P
Approval Date: 2024-11-29
Registrant: ABBVIE PTE. LTD.
Drug Type: Therapeutic
Forensic Classification: Prescription Only
Dosage Form: TABLET
Route Of Administration: ORAL
Atc Code: N02CD07
Pharma Manufacturer Name: ABBVIE PTE. LTD.
Company Detail Path: /organization/06965e897de37e6f/abbvie-pte-ltd

Active Ingredients

Atogepant monohydrate eqv Atogepant

60.0mg

Atogepant monohydrate eqv Atogepant

60.0mg

Approved

Quick Info

Agency

HSA

Country

🇸🇬

Approval Date

Nov 29, 2024

Approval ID

ad008fab522859fe

Type

Therapeutic

Back to HSA Approvals