DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1M/s Dr. Reddy's Laboratories
02 1M/s Asolution Pharmaceuticals Pvt ltd
03 1Shandong Chenghui Shuangda Pharmaceutical Co., Ltd
04 1M/s. Neuland Laboratories Ltd
05 1USV Private Limited
06 1M/s Almelo Private Limited
07 1M/s Azico Biophore India
08 1M/s Azico Biophore India Pvt Ltd
09 1M/s MSN Laboratories
10 1M/s. Apicore Pharmaceuticals Pvt. Ltd.,
11 1M/s. Natco Pharma Ltd,
12 1M/sNatco Pharma Limited
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm : Chemical Technical Operations Unit-VI, APIIC Industrial Estate, Pydibhimavaram V...
ASolution Pharmaceuticals: Your Partner for cGMP Development & Manufacturing Services – Supplying APIs, FDFs, and Specialty Molecules.
Date of Issue : 2024-01-23
Valid Till : 2026-06-17
Written Confirmation Number : WC-476
Address of the Firm : K3/8 Anand Nagar, MIDC, Ambernath-421506 District Thane, Maharshtra
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
Date of Issue : 2023-04-07
Valid Till : 2026-04-06
Written Confirmation Number : SD230030
Address of the Firm : Economic Development Zone, Pingyuan County, Dezhou City, Shandong, PR China
Neuland Laboratories- A dedicated 100% API provider.
Date of Issue : 2022-07-28
Valid Till : 2025-06-16
Written Confirmation Number : WC-0036
Address of the Firm : Unit-1, Sy. No. 347, 473, 474, 490/2, Bonthapally Village, Veerabhadraswamy, Tem...
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
Date of Issue : 2022-06-27
Valid Till : 2025-06-02
Written Confirmation Number : WC-0012
Address of the Firm : MIs USV Private Limited ,B-1/8,MIDC, Lote Parshuram, Tal., Dist. Ratnagiri, Khed...
A Sugammadex Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sugammadex Sodium, including repackagers and relabelers. The FDA regulates Sugammadex Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sugammadex Sodium API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Sugammadex Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sugammadex Sodium supplier is an individual or a company that provides Sugammadex Sodium active pharmaceutical ingredient (API) or Sugammadex Sodium finished formulations upon request. The Sugammadex Sodium suppliers may include Sugammadex Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Sugammadex Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Sugammadex Sodium written confirmation (Sugammadex Sodium WC) is an official document issued by a regulatory agency to a Sugammadex Sodium manufacturer, verifying that the manufacturing facility of a Sugammadex Sodium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Sugammadex Sodium APIs or Sugammadex Sodium finished pharmaceutical products to another nation, regulatory agencies frequently require a Sugammadex Sodium WC (written confirmation) as part of the regulatory process.
click here to find a list of Sugammadex Sodium suppliers with Written Confirmation (WC) on PharmaCompass.
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