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Approvals
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Zukastop
Approved
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Zukastop
Stallion Laboratories Pvt. Ltd
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
314d317777533727
Company
Stallion Laboratories Pvt. Ltd
Type
Standard
Approval Details
Approval Id
314d317777533727
Drug Approval Philippines Name
Zukastop
Product Name
Zukastop
Registration Number
DRP-6609-06
Brand Name
Zukastop
Generic Name
Ondansetron (as hydrochloride dihydrate)
Dosage Form
Film-Coated Tablet
Dosage Strength
8 mg
Manufacturer
Stallion Laboratories Pvt. Ltd
Importer
Ambica International Corporation
Distributor
Ellebasy Medicale Group Inc
Issuance Date
26 April 2025
Expiry Date
26 April 2037
Pharmacologic Category
Antiemetic (5-HT3-Receptor Antagonist)
Classification
Prescription Drug (Rx)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
314d317777533727
Type
Standard
Back to Philippines FDA Approvals
Zukastop - Philippines FDA Drug Approval Details