Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
01 1Cohance Lifesciences Limited
02 1Dr.Reddy's Laboratories Limited
03 1Neuland Laboratories Limited
04 1USV Private Limited
05 1Teva API India Private Ltd
06 1Alembic Pharmaceuticals Limited
07 1AstraZeneca AB
08 1CTX Lifesciences Pvt. Ltd.
09 1Divi's Laboratories Limited
10 1Honour Lab Limited
11 1Jubilant Pharmova Limited
12 1Lonza AG
13 2MSN Organics Private Limited
14 1Micro Labs Limited
15 1Patheon Austria GmbH & CoKG
16 1Sichuan Qingmu Pharmaceutical Co., Ltd.
17 1Tianish Laboratories Private Limited
18 1Unichem Laboratories Limited, India
19 1Viyash Life Sciences Private Limited
20 1YiChang HEC ChangJiang Pharmaceuical Co.,Ltd.
21 1Zhejiang Hisun Pharmaceutical Co., Ltd.
22 1n.v.Ajinomoto Ominchem
01 4TICAGRELOR
02 15Ticagrelor
03 4ticagrelor
01 1Belgium
02 3China
03 15India
04 1Israel
05 2U.S.A
06 1United Kingdom
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
NDC Package Code : 76072-1016
Start Marketing Date : 2019-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-969
Start Marketing Date : 2014-08-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-2032
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 : 62147-0280
Start Marketing Date : 2021-12-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
NDC Package Code : 15894-0030
Start Marketing Date : 2015-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46708-883
Start Marketing Date : 2016-09-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17228-7777
Start Marketing Date : 2014-02-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42419-030
Start Marketing Date : 2024-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42571-282
Start Marketing Date : 2015-02-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45941-3055
Start Marketing Date : 2014-10-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Brilinta manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Brilinta, including repackagers and relabelers. The FDA regulates Brilinta manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Brilinta 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 Brilinta manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Brilinta supplier is an individual or a company that provides Brilinta active pharmaceutical ingredient (API) or Brilinta finished formulations upon request. The Brilinta suppliers may include Brilinta API manufacturers, exporters, distributors and traders.
click here to find a list of Brilinta 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 Brilinta as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Brilinta 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 Brilinta 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 Brilinta and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Brilinta NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Brilinta suppliers with NDC on PharmaCompass.
We have 22 companies offering Brilinta
Get in contact with the supplier of your choice:
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