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Flexall Ultra - SFDA Drug Approval Details

Approvals/SFDA/Flexall Ultra

Authorized

GENERIC

Flexall Ultra

Unknown🇸🇦 Saudi Food and Drug Authority

Approval Date: N/A
Approval ID: 59e8fcbca1d75ad0
Company: Unknown
Type: Generic

Approval Details

Approval Id: 59e8fcbca1d75ad0
Drug Approval Sfda Name: Flexall Ultra
Trade Name: Flexall Ultra
Generic Name: GLUCOSAMINE HYDROCHLORIDE,METHYLSULFONYLMETHANE,CALCIUM FRUCTOBORATE,CHONDROITIN,SODIUM HYALURONATE
Register Number: 0806233778
Register Year: 2023
Drug Type: Generic
Route Of Administration: Oral use
Package Type: Bottle
Package Size: 120
Legal Status: OTC
Authorization Status: Valid
Marketing Status: Marketed
Product Control: Uncontrolled
Storage Conditions: do not store above 30°c
Shelf Life: 24 Months
Distribution Site: Pharmacy
Description Code: 35000011506-1139.8-100000073665
Price: 109.2

Active Ingredients

Authorized

Quick Info

Agency

SFDA

Country

🇸🇦

Approval ID

59e8fcbca1d75ad0

Type

Generic

Back to SFDA Approvals