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01 1Symbiotec Pharmalab Private Limited

02 1Aurisco Pharmaceutical Co.,Ltd

03 1Aurobindo Pharma Limited

04 1Catalent Micron Technologies, Inc.

05 2Chemo Biosynthesis s.r.l.

06 1Curia Spain, S.A.U.

07 1Hetero Labs Limited

08 1Hubei Biocause Heilen Pharmaceutical Co., Ltd

09 1Industriale Chimica s.r.l.

10 1Janssen Pharmaceutica NV

11 2MSN Laboratories Private Limited

12 1Olon S.p.A.

13 2Olon SpA

14 1Quimica Sintetica S.A.

15 1Raks Pharma Pvt. Limited

16 1SHILPA PHARMA LIFESCIENCES LIMITED

17 2STERLING SPA

18 1ScinoPharm Taiwan Ltd.

19 1Sicor S.r.l.

20 1Sicor de Mexico S.A. de C.V

21 2Sterling Chemical Malta Ltd

22 1Tianjin Pacific Chemical and Pharmaceutical Co. Ltd.

23 1Zhejiang Shenzhou Pharmaceutical Co., Ltd

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSymbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.

ABIRATERONE ACETATE

NDC Package Code : 22552-0035

Start Marketing Date : 2013-06-04

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

Symbiotec Pharmalab

02

BioProcess International Europe
Not Confirmed
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BioProcess International Europe
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ABIRATERONE ACETATE

NDC Package Code : 16812-004

Start Marketing Date : 2021-09-23

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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03

BioProcess International Europe
Not Confirmed
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BioProcess International Europe
Not Confirmed

ABIRATERONE ACETATE

NDC Package Code : 12578-619

Start Marketing Date : 2011-04-28

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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04

BioProcess International Europe
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05

BioProcess International Europe
Not Confirmed
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06

BioProcess International Europe
Not Confirmed
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07

BioProcess International Europe
Not Confirmed
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BioProcess International Europe
Not Confirmed

ABIRATERONE ACETATE

NDC Package Code : 53069-1030

Start Marketing Date : 2018-05-22

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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08

BioProcess International Europe
Not Confirmed
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BioProcess International Europe
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ABIRATERONE ACETATE

NDC Package Code : 47621-043

Start Marketing Date : 2013-06-30

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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09

BioProcess International Europe
Not Confirmed
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BioProcess International Europe
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ABIRATERONE ACETATE

NDC Package Code : 26251-0004

Start Marketing Date : 2017-12-06

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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10

BioProcess International Europe
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BioProcess International Europe
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ABIRATERONE ACETATE

NDC Package Code : 16637-0050

Start Marketing Date : 2022-01-11

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 154229-18-2 / Abiraterone Acetate API manufacturers, exporters & distributors?

Abiraterone Acetate manufacturers, exporters & distributors 1

23

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

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

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

API | Excipient name

Abiraterone Acetate

Synonyms

154229-18-2, Zytiga, Cb7630, Cb-7630, Yonsa, Cb 7630

Cas Number

154229-18-2

Unique Ingredient Identifier (UNII)

EM5OCB9YJ6

About Abiraterone Acetate

An androstene derivative that inhibits STEROID 17-ALPHA-HYDROXYLASE and is used as an ANTINEOPLASTIC AGENT in the treatment of metastatic castration-resistant PROSTATE CANCER.

Zytiga Manufacturers

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

Zytiga Suppliers

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

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

Zytiga 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 Zytiga as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Zytiga 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.