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01 1Dr. Reddy's Laboratories Limited

02 1Aspen Oss B.V.

03 1Wavelength Enterprises LTD

04 1Medichem Manufacturing (Malta) Ltd.

05 1Medichem S.A.

06 1Neuland Laboratories Limited

07 1USV Private Limited

08 1Farmhispania S.A.

09 1APICORE PHARMACEUTICALS PRIVATE LIMITED

10 1Aurobindo Pharma Limited

11 1Azico Biophore India Private Limited

12 1BrightGene Bio-Medical Technology Co., Ltd.

13 3F.I.S. - Fabbrica Italiana Sintetici S.p.A.

14 1Honour Lab Limited

15 1MSN Life Sciences Private Limited

16 1Natco Pharma Limited

17 1Pharma Source Direct, Inc.

18 1SOLARA ACTIVE PHARMA SCIENCES LIMITED

19 1ScinoPharm Taiwan Ltd.

20 1TAPI Croatia Industries Ltd.

21 1Teva Pharmaceutical Works Private Limited Company

22 3Zhejiang Ausun Pharmaceutical Co., Ltd.

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

SUGAMMADEX SODIUM

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

Dr Reddy Company Banner

02

SUGAMMADEX

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

Aspen API Comapny Banner

03

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSeqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.

SUGAMMADEX

NDC Package Code : 58175-0618

Start Marketing Date : 2018-08-30

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Seqens Company Banner

04

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMedichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.

SUGAMMADEX SODIUM

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

Medichem

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNeuland Laboratories- A dedicated 100% API provider.

SUGAMMADEX

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

Neuland

06

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothUSV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.

SUGAMMADEX SODIUM

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

USV Private Limited

07

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothFarmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.

SUGAMMADEX

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

Farmhispania

08

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PharmaVenue
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMedichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.

SUGAMMADEX SODIUM

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

Medichem

09

PharmaVenue
Not Confirmed
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PharmaVenue
Not Confirmed

SUGAMMADEX

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

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10

TAPI Croatia Industries Ltd.

Country
PharmaVenue
Not Confirmed
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TAPI Croatia Industries Ltd.

Country
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PharmaVenue
Not Confirmed

SUGAMMADEX SODIUM

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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Sugammadex Sodium Manufacturers

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.

Sugammadex Sodium Suppliers

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.

Sugammadex Sodium NDC

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).

Finished drug products

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.

Unfinished drugs

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.

Compounded drug products

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.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.