Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 1,374Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1INKE SA

02 1Dr. Reddy's Laboratories Limited

03 1Glaxo Wellcome Manufacturing Pte. Ltd

04 1HIKAL LIMITED

05 1Hikma Pharmaceuticals

06 1Ipca Laboratories Limited

07 1SUN PHARMACEUTICAL INDUSTRIES, INC.

08 1ScinoPharm Taiwan Ltd.

09 1TAPI Hungary Industries Kft.

10 1Teva Pharmaceutical Works Private Limited Company

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothInke S.A: APIs manufacturing plant.

ONDANSETRON

NDC Package Code : 64567-0008

Start Marketing Date : 2009-08-19

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Inke Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

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

ONDANSETRON, (3R)-

NDC Package Code : 55111-050

Start Marketing Date : 2010-01-01

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

03

AMWC Asia-TDAC
Not Confirmed
arrow

04

AMWC Asia-TDAC
Not Confirmed
arrow
arrow
AMWC Asia-TDAC
Not Confirmed

ONDANSETRON

NDC Package Code : 66651-904

Start Marketing Date : 2015-01-23

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

blank

05

AMWC Asia-TDAC
Not Confirmed
arrow
arrow
AMWC Asia-TDAC
Not Confirmed

ONDANSETRON

NDC Package Code : 59115-807

Start Marketing Date : 2019-01-01

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

blank

07

AMWC Asia-TDAC
Not Confirmed
arrow

08

AMWC Asia-TDAC
Not Confirmed
arrow
arrow
AMWC Asia-TDAC
Not Confirmed

ONDANSETRON

NDC Package Code : 62756-469

Start Marketing Date : 2025-03-11

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

blank

09

AMWC Asia-TDAC
Not Confirmed
arrow
arrow
AMWC Asia-TDAC
Not Confirmed

ONDANSETRON

NDC Package Code : 51846-1033

Start Marketing Date : 2017-11-17

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

blank

10

TAPI Hungary Industries Kft.

Country
AMWC Asia-TDAC
Not Confirmed
arrow

TAPI Hungary Industries Kft.

Country
arrow
AMWC Asia-TDAC
Not Confirmed

ONDANSETRON

NDC Package Code : 84671-1033

Start Marketing Date : 2017-11-17

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

blank

Looking for 99614-02-5 / Ondansetron API manufacturers, exporters & distributors?

Ondansetron manufacturers, exporters & distributors 1

46

PharmaCompass offers a list of Ondansetron 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 Ondansetron manufacturer or Ondansetron supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ondansetron manufacturer or Ondansetron supplier.

PharmaCompass also assists you with knowing the Ondansetron API Price utilized in the formulation of products. Ondansetron API Price is not always fixed or binding as the Ondansetron Price is obtained through a variety of data sources. The Ondansetron Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Ondansetron

Synonyms

99614-02-5, Zofran, Zudan, 9-methyl-3-((2-methyl-1h-imidazol-1-yl)methyl)-2,3-dihydro-1h-carbazol-4(9h)-one, Zofran odt, Zuplenz

Cas Number

99614-02-5

Unique Ingredient Identifier (UNII)

4AF302ESOS

About Ondansetron

A competitive serotonin type 3 receptor antagonist. It is effective in the treatment of nausea and vomiting caused by cytotoxic chemotherapy drugs, including cisplatin, and has reported anxiolytic and neuroleptic properties.

Zofran ODT Manufacturers

A Zofran ODT manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zofran ODT, including repackagers and relabelers. The FDA regulates Zofran ODT manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zofran ODT 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 Zofran ODT manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Zofran ODT Suppliers

A Zofran ODT supplier is an individual or a company that provides Zofran ODT active pharmaceutical ingredient (API) or Zofran ODT finished formulations upon request. The Zofran ODT suppliers may include Zofran ODT API manufacturers, exporters, distributors and traders.

click here to find a list of Zofran ODT suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Zofran ODT 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 Zofran ODT as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Zofran ODT 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 Zofran ODT 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 Zofran ODT and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zofran ODT NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Zofran ODT suppliers with NDC on PharmaCompass.

Zofran ODT Manufacturers | Traders | Suppliers

Zofran ODT Manufacturers, Traders, Suppliers 1
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.