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NEUPRO 4 MG/24 HRS TRANSDERMAL PATCHES - SFDA Drug Approval Details

Approvals/SFDA/NEUPRO 4 MG/24 HRS TRANSDERMAL PATCHES

Authorized

NCE

NEUPRO 4 MG/24 HRS TRANSDERMAL PATCHES

Unknown🇸🇦 Saudi Food and Drug Authority

Approval Date: N/A
Approval ID: ad9d08fd5640f58e
Company: Unknown
Type: NCE

Approval Details

Approval Id: ad9d08fd5640f58e
Drug Approval Sfda Name: NEUPRO 4 MG/24 HRS TRANSDERMAL PATCHES
Trade Name: NEUPRO 4 MG/24 HRS TRANSDERMAL PATCHES
Generic Name: ROTIGOTINE
Register Number: 0903257011
Register Year: 2020
Drug Type: NCE
Route Of Administration: Transdermal use
Package Type: Patch
Package Size: 28
Legal Status: Prescription
Authorization Status: Valid
Marketing Status: Marketed
Product Control: Uncontrolled
Storage Conditions: store below 30°c
Shelf Life: 30 Months
Distribution Site: Pharmacy
Description Code: 7000001122-4-100000073741
Price: 219

Active Ingredients

Authorized

Quick Info

Agency

SFDA

Country

🇸🇦

Approval ID

ad9d08fd5640f58e

Type

NCE

Back to SFDA Approvals