DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Granules India Limited
03 1Apicore Pharmaceuticals Private Limited
04 1Apicore US LLC
05 1Ash Stevens LLC
06 1BSP Pharmaceuticals
07 1Cilag AG
08 1Hetero Labs Limited
09 1Hubei Honch Pharmaceutical Co., Ltd.
10 1Jiangsu Hansoh Pharmaceutical Group Co., Ltd.
11 1Laurus Labs Limited
12 1MSN Laboratories Private Limited
13 1NATCO PHARMA LIMITED
14 1Qilu Pharmaceutical Co. Ltd.
15 1SHILPA PHARMA LIFESCIENCES LIMITED
16 1SUN PHARMACEUTICAL INDUSTRIES, INC.
17 1SciAnda (Changshu) Pharmaceuticals, Ltd.
18 2ScinoPharm Taiwan Ltd.
19 1Sionc Pharmaceutical Private Limited
20 1TAPI Czech Industries s.r.o.
21 1Teva Czech Industries s.r.o
01 4BORTEZOMIB
02 16Bortezomib
03 1Bortezomib 3.5mg/vial
04 1bortezomib
01 3China
02 11India
03 1Israel
04 1Italy
05 1Switzerland
06 3Taiwan
07 1U.S.A
08 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-922
Start Marketing Date : 2012-07-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-972
Start Marketing Date : 2021-04-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14096-140
Start Marketing Date : 2009-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42973-140
Start Marketing Date : 2009-11-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48957-0018
Start Marketing Date : 2003-05-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43624-024
Start Marketing Date : 2003-05-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (3.5mg/3.5mg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 12502-5268
Start Marketing Date : 2010-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42385-716
Start Marketing Date : 2012-12-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54245-7004
Start Marketing Date : 2013-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-031
Start Marketing Date : 2014-09-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Velcade manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Velcade, including repackagers and relabelers. The FDA regulates Velcade manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Velcade 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 Velcade manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Velcade supplier is an individual or a company that provides Velcade active pharmaceutical ingredient (API) or Velcade finished formulations upon request. The Velcade suppliers may include Velcade API manufacturers, exporters, distributors and traders.
click here to find a list of Velcade 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 Velcade as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Velcade 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 Velcade 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 Velcade and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Velcade NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Velcade suppliers with NDC on PharmaCompass.
We have 18 companies offering Velcade
Get in contact with the supplier of your choice:
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