
Rotigotine Patch
Form: Patches
Strength: 2 mg/24 hr, 4 mg/24 hr, 6 mg/24 hr, 8 mg/24 hr, and 12 mg/24 hr
Reference Brands: Neupro
Category: Transdermal Patches
Rotigotine transdermal patches (Neupro) are regulated in the EU and US, supported by dossiers demonstrating safety, efficacy, and manufacturing quality in compliance with GMP and MDR standards. In the US, FDA approval involved extensive clinical validation and safety assessments, while in the EU, CE marking certifies conformity with MDR standards. These products undergo validation, stability testing, and audits, with comprehensive documentation including safety profiles, clinical trial data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to reliable, approved rotigotine patches supporting Parkinson’s disease and RLS treatment worldwide, improving patient outcomes and healthcare safety.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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