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hydroxyprophylmethylcellulose

Eye drops 0.5 % - 10 ml

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #11938
A pharmaceutical manufacturer focused on high-complexity and rare-disease care, supplying pharmaceutical products for low-prevalence conditions such as inherited metabolic disorders and tuberculosis, alongside a growing line of OTX and nutraceutical pharmaceutical products for areas including cardiometabolic, neuro-geriatric, respiratory, cellular oxidation, and aesthetic/vascular medicine. The company combines ethical prescription medicines with foods for special medical purposes to support long-term patient management, and highlights a quality culture where raw materials are selected to meet ISO/GMP standard requirements across its pharmaceutical products portfolio.

Manufacturer usually replies in 38 days

hydroxyprophylmethylcellulose

Eye drops 3mg

Dossier type
EU CTD
Dossier status
Ready to file
Country of origin
European Union
GMP approvals
EU GMP
Manufacturer #1183
This company is a leading global manufacturer of ophthalmology products, as well as medical devices and nutritional supplements. They adhere to the highest quality standards, emphasizing GMP certifications. Their product portfolio includes prescription medications, over-the-counter drugs, and dietary supplements, with a strong focus on three key therapy areas: eye health, allergy relief, and inflammation management. Principal dosage forms include drops, sprays, granules, and masks. They hold several product patents and are active in regions such as the EU, North America, and Southeast Asia.

Manufacturer usually replies in 44 days

glycerol + hydroxyprophylmethylcellulose + polyethylene glycol

Eye drops 0.2%+0.2%+1%

Dossier type
CTD
Dossier status
Ready to file
Country of origin
South Korea
GMP approvals
EU GMP
Manufacturer #11554
It is the leading pharmaceutical company specializing in ophthalmic products. The company has acquired EU GMP certification and has been under preparation for CGMP approval for both manufacturing sites of multi-dose and single-dose products.

Manufacturer usually replies in 4 days

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