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DUSPAMEN 200 mg prolonged release capsule - SFDA Drug Approval Details

Approvals/SFDA/DUSPAMEN 200 mg prolonged release capsule

Authorized

GENERIC

DUSPAMEN 200 mg prolonged release capsule

Unknown🇸🇦 Saudi Food and Drug Authority

Approval Date: N/A
Approval ID: ba45311df264f4b3
Company: Unknown
Type: Generic

Approval Details

Approval Id: ba45311df264f4b3
Drug Approval Sfda Name: DUSPAMEN 200 mg prolonged release capsule
Trade Name: DUSPAMEN 200 mg prolonged release capsule
Generic Name: MEBEVERINE HYDROCHLORIDE
Register Number: 354-334-20
Register Year: 2020
Drug Type: Generic
Route Of Administration: Oral use
Package Type: Blister
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: 7000000797-200-100000073668
Price: 40.9

Active Ingredients

Authorized

Quick Info

Agency

SFDA

Country

🇸🇦

Approval ID

ba45311df264f4b3

Type

Generic

Back to SFDA Approvals