tazarotene Cutaneous gel 0.1%

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #16299
The company has a manufacturer’s license for medicinal products for human use authorized by the National Agency of Medicines. The highest quality products are manufactured and packaged in the production units with GMP International Standards and regularly checked by the National Agency of Medicines by the requirements of the European Medicines Agency (EMEA). The principal activity of the company is the production of pharmaceutical products, which are certified with patents, in various forms (tablets, capsules, syrups, oral solutions, powders for liquid compositions, gels, creams, and ointments) and various categories (antibiotics, antifungals, antivirals, anti-inflammatories, analgesics, antipyretics, anxiolytics, antidepressants, bronchodilators, antilipidemics, antitussives, cholinesterase inhibitors, antipsoriatics, antacids, anticholinergics, antidiarrheals, etc.).

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