Fluoxetine Pellets And Powder

Form: Pellets: Oral, slow-release formulations for capsule manufacturing; Powder: Used in pharmaceutical manufacturing for capsule or suspension fabrication

Strength: Supplied as high-purity API in pellet and powder forms

Reference Brands: Prozac and Generic fluoxetine

Category: Active Pharmaceutical Ingredient

Fluoxetine pellets and powder are regulated in the EU and US, with dossiers demonstrating safety, efficacy, and manufacturing quality in accordance with GMP standards. In the US, FDA approval involves clinical validation, safety testing, and GMP compliance. In the EU, CE marking certifies conformity with MDR standards. These products undergo validation, stability testing, and audits, supported by detailed documentation including safety profiles, pharmacological data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to high-quality fluoxetine API, supporting the production of antidepressant formulations and mental health therapies globally.