
Praziquantel injection
Form: Injection
Strength: 56.8 mg/ml
Reference Brands: Droncit & Generic formulations for this form in EU & US
Category: Veterinary Product
Praziquantel injection is authorized in the EU and US, supported by dossiers demonstrating safety, efficacy, and manufacturing quality according to GMP standards. In the US, FDA approval requires extensive clinical data and safety evaluation, while in the EU, CE marking certifies conformity with veterinary medicinal product regulations. These products undergo validation, stability testing, and quality audits, with detailed documentation including safety profiles, clinical trial data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring regulatory compliance guarantees access to safe, effective praziquantel formulations for treating parasitic infections in animals worldwide.
The Trade Mark owner has been correctly identified under the heading Manufacturer / TM Owner as required by the Act.
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