DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Aspen Oss B.V.
03 1Medichem Manufacturing (Malta) Ltd.
04 1Medichem S.A.
05 1Neuland Laboratories Limited
06 1USV Private Limited
07 1Farmhispania S.A.
08 1APICORE PHARMACEUTICALS PRIVATE LIMITED
09 1Aurobindo Pharma Limited
10 1Azico Biophore India Private Limited
11 1BrightGene Bio-Medical Technology Co., Ltd.
12 3F.I.S. - Fabbrica Italiana Sintetici S.p.A.
13 1Honour Lab Limited
14 1MSN Life Sciences Private Limited
15 1Natco Pharma Limited
16 1Pharma Source Direct, Inc.
17 1SOLARA ACTIVE PHARMA SCIENCES LIMITED
18 1ScinoPharm Taiwan Ltd.
19 1TAPI Croatia Industries Ltd.
20 1Teva Pharmaceutical Works Private Limited Company
21 3Zhejiang Ausun Pharmaceutical Co., Ltd.
01 2SUGAMMADEX
02 1SUGAMMADEX CRUDE
03 2SUGAMMADEX SODIUM
04 1SUGGAMADEX SODIUM
05 3Sugammadex
06 16Sugammadex Sodium
01 4China
02 10India
03 1Israel
04 3Italy
05 1Netherlands
06 3Spain
07 1Taiwan
08 1U.S.A
09 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 71796-003
Start Marketing Date : 2019-11-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Aspen API. More than just an API™
NDC Package Code : 60870-0464
Start Marketing Date : 2015-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
NDC Package Code : 16436-0119
Start Marketing Date : 2017-11-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-2031
Start Marketing Date : 2019-11-13
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
NDC Package Code : 62147-0278
Start Marketing Date : 2019-12-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
NDC Package Code : 17404-1030
Start Marketing Date : 2023-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
NDC Package Code : 53296-0119
Start Marketing Date : 2017-11-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-233
Start Marketing Date : 2017-07-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0151
Start Marketing Date : 2020-03-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11722-068
Start Marketing Date : 2019-05-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Sugammadex Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Sugammadex Sodium manufacturer or Sugammadex Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Sugammadex Sodium manufacturer or Sugammadex Sodium supplier.
PharmaCompass also assists you with knowing the Sugammadex Sodium API Price utilized in the formulation of products. Sugammadex Sodium API Price is not always fixed or binding as the Sugammadex Sodium Price is obtained through a variety of data sources. The Sugammadex Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
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.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Sugammadex Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sugammadex Sodium API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Sugammadex Sodium as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Sugammadex Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sugammadex Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sugammadex Sodium suppliers with NDC on PharmaCompass.
We have 19 companies offering Sugammadex Sodium
Get in contact with the supplier of your choice:
