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VYZULTA - SFDA Drug Approval Details

Approvals/SFDA/VYZULTA

Authorized

NCE

VYZULTA

Unknown🇸🇦 Saudi Food and Drug Authority

Approval Date: N/A
Approval ID: 43fcbb20ffb7352e
Company: Unknown
Type: NCE

Approval Details

Approval Id: 43fcbb20ffb7352e
Drug Approval Sfda Name: VYZULTA
Trade Name: VYZULTA
Generic Name: LATANOPROSTENE BUNOD
Register Number: 2312246473
Register Year: 2024
Drug Type: NCE
Route Of Administration: Ophthalmic use
Package Type: Bottle
Package Size: 1
Size: 5
Size Unit: ml
Legal Status: Prescription
Authorization Status: Valid
Marketing Status: Marketed
Product Control: Uncontrolled
Storage Conditions: store in a refrigerator (2°c – 8°c)
Shelf Life: 36 Months
Distribution Site: Pharmacy
Description Code: 7000002767-0.024-100000073759
Price: 92.05

Active Ingredients

Authorized

Quick Info

Agency

SFDA

Country

🇸🇦

Approval ID

43fcbb20ffb7352e

Type

NCE

Back to SFDA Approvals