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Valsartan manufacturers

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Country of origin : Oman

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7 products found

sacubitril + valsartan

Tablets 24 mg + 26 mg, 49 mg + 51 mg, 97 mg + 103 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
Oman
GMP approvals
FDA, EU GMP, South Africa
Comments
API CEP/EU compliant. Ref. Entresto, Novartis
Manufacturer #20781

​Established in 2001, this Manufacturer is a CTD dossier owner and manufacturer with a global presence spanning over 45 countries and regions. With a dedicated team of 501–1,000 employees, it operates GMP-certified facilities in Oman, producing a diverse range of products including tablets, capsules, creams, balms, external liquids, and powder sachets. As a GMP manufacturer, it holds certifications from authorities such as US-FDA, MHRA-UK, TGA-Australia, GCC-DR, and ANVISA-Brazil, ensuring adherence to international quality standards. The Manufacturer's commitment to excellence as a CTD dossier owner and manufacturer and GMP manufacturer solidifies its reputation in the global pharmaceutical market.​

Manufacturer usually replies in 23 days

amlodipine + valsartan

Tablets 5 mg + 320 mg, 10 mg + 320 mg

Dossier type
EU CTD
Dossier status
Under development
Country of origin
Oman
GMP approvals
FDA, EU GMP, South Africa
Manufacturer #20781

​Established in 2001, this Manufacturer is a CTD dossier owner and manufacturer with a global presence spanning over 45 countries and regions. With a dedicated team of 501–1,000 employees, it operates GMP-certified facilities in Oman, producing a diverse range of products including tablets, capsules, creams, balms, external liquids, and powder sachets. As a GMP manufacturer, it holds certifications from authorities such as US-FDA, MHRA-UK, TGA-Australia, GCC-DR, and ANVISA-Brazil, ensuring adherence to international quality standards. The Manufacturer's commitment to excellence as a CTD dossier owner and manufacturer and GMP manufacturer solidifies its reputation in the global pharmaceutical market.​

Manufacturer usually replies in 23 days

valsartan

Tablets 80 mg, 160 mg

Dossier type
CTD
Dossier status
Ready to file
Country of origin
Oman
GMP approvals
FDA
Manufacturer #20781

​Established in 2001, this Manufacturer is a CTD dossier owner and manufacturer with a global presence spanning over 45 countries and regions. With a dedicated team of 501–1,000 employees, it operates GMP-certified facilities in Oman, producing a diverse range of products including tablets, capsules, creams, balms, external liquids, and powder sachets. As a GMP manufacturer, it holds certifications from authorities such as US-FDA, MHRA-UK, TGA-Australia, GCC-DR, and ANVISA-Brazil, ensuring adherence to international quality standards. The Manufacturer's commitment to excellence as a CTD dossier owner and manufacturer and GMP manufacturer solidifies its reputation in the global pharmaceutical market.​

Manufacturer usually replies in 23 days

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SACUBITRIL Manufacturers

Sacubitril is a medical substance also known as neprilysin inhibitor that is used in combination with valsartan as an aide to decrease the chance of cardiovascular passing and hospitalization for heart disappointment in patients with incessant heart disappointment (NYHA Course II-IV) and diminished discharge division. Warnings: Follow all Instructions on your medicine package and label. It is wise to tell your healthcare providers about all your medical allergies, illnesses, and all medicines you use. Before taking SACUBITRIL: You should not use This medical remedy if you are allergic to it This drug may also be used for purposes that may not have been listed in this medication guide.

How does SACUBITRIL work?

Sacubitril's dynamic metabolite, LBQ657 hinders neprilysin, an unbiased endopeptidase that would regularly cleave natriuretic peptides, which incorporate: atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), and c-type natriuretic peptide (CNP).

The Wholesale Price of SACUBITRIL

It is obtainable in generic and brand versions. It is not covered by most Medicare and insurance plans, but pharmacy coupons can help balance the price. The cost for SACUBITRIL oral tablet (24 mg-26 mg) is around $618 for a supply of 60 tablets. Prices may vary on the pharmacy you visit.

Navigating our pharmaceutical marketplace

Being a global B2B pharmaceutical online marketplace, Pipelinepharma is structured to simplify pharmaceutical deals by providing you with an intuitive interface that is easy to engage with. The selection of SACUBITRIL offerings can be narrowed down with the use of filters and easily weighed against one another according to medication prices and commercial terms. The advanced filters help you filter out the countries for SACUBITRIL manufacturers and SACUBITRIL suppliers that you are looking for. These also enable you to check the dossier status of Valaciclovir, and the GMP approvals of the different variants of Valaciclovir. Also, each manufacturer or supplier product description contains essential information about SACUBITRIL including clinical data, stability zones, countries where SACUBITRIL is already registered in. Manufacturers also have special, and delivery terms.

Establishing commercial ties

If you are a pharmaceutical licensing company or a distributor you can enter into deals or negotiations over Ivermectin offers with manufacturing companies after completing the free registration process and joining our online marketplace. This helps to ensure that you conclude the pharmaceutical deal at a reasonable cost and achieve the best cost/benefit ratio for your company while bypassing lengthy sourcing, negotiation, and ordering process. Once you have finalized a deal, you can look forward to a long-lasting business relationship with the manufacturers or suppliers. This way, the marketplace allows you as a distributor to skip the process of shortlisting product manufacturers every time you are looking for in-licensing or distribution deals.

Quality Assurance

To keep up to the quality standards other than Good Manufacturing Practice approvals that Ivermectin manufacturers have, we qualify their companies before they are onboarded on the platform. This allows us to screen Ivermectin manufacturers for the quality of the pharmaceutical products’ dossiers and protect against the risk of possible malpractices.

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