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TEBARAT - SFDA Drug Approval Details

Approvals/SFDA/TEBARAT

Authorized

NCE

TEBARAT

Unknown🇸🇦 Saudi Food and Drug Authority

Approval Date: N/A
Approval ID: 797fb82bc7c29cf3
Company: Unknown
Type: NCE

Approval Details

Approval Id: 797fb82bc7c29cf3
Drug Approval Sfda Name: TEBARAT
Trade Name: TEBARAT
Generic Name: AZELASTINE
Register Number: 1-5355-19
Register Year: 2021
Drug Type: NCE
Route Of Administration: Ocular use
Package Type: Ampoule
Package Size: 30
Legal Status: Prescription
Authorization Status: Valid
Marketing Status: Marketed
Product Control: Uncontrolled
Storage Conditions: store below 30°c
Shelf Life: 24 Months
Distribution Site: Pharmacy
Description Code: 7000000111-0.5-200000016460
Price: 38.7

Active Ingredients

Authorized

Quick Info

Agency

SFDA

Country

🇸🇦

Approval ID

797fb82bc7c29cf3

Type

NCE

Back to SFDA Approvals