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01 1Farmabios S.p.A.
02 1Granules India Limited
03 2Apothecon Pharmaceuticals Pvt Ltd
04 1Aurobindo Pharma Limited
05 1Chemcon, GmbH
06 1Emcure Pharmaceuticals Limited
07 1Hetero Labs Limited
08 1Hubei Honch Pharmaceutical Co., Ltd.
09 1Olon SpA
10 1Patheon Manufacturing Services LLC
11 1SHILPA PHARMA LIFESCIENCES LIMITED
12 1Sionc Pharmaceutical Private Limited
13 1Zhejiang ChemPacific Corporation
01 2MELPHALAN HYDROCHLORIDE
02 2Melphalan HCl
03 10Melphalan Hydrochloride
01 1China
02 2Germany
03 8India
04 1Italy
05 2U.S.A
NDC Package Code : 46439-8735
Start Marketing Date : 2011-05-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
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 : 62207-978
Start Marketing Date : 2021-08-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-684
Start Marketing Date : 2023-12-06
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64757-0013
Start Marketing Date : 2011-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59981-016
Start Marketing Date : 2010-10-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-847
Start Marketing Date : 2023-12-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0087
Start Marketing Date : 1992-11-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62158-0007
Start Marketing Date : 2021-02-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0304
Start Marketing Date : 2010-04-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63552-076
Start Marketing Date : 2016-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION (50mg/10mL)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Melphalan Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Melphalan Hydrochloride, including repackagers and relabelers. The FDA regulates Melphalan Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Melphalan Hydrochloride 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 Melphalan Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Melphalan Hydrochloride supplier is an individual or a company that provides Melphalan Hydrochloride active pharmaceutical ingredient (API) or Melphalan Hydrochloride finished formulations upon request. The Melphalan Hydrochloride suppliers may include Melphalan Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Melphalan Hydrochloride 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 Melphalan Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Melphalan Hydrochloride 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 Melphalan Hydrochloride 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 Melphalan Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Melphalan Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Melphalan Hydrochloride suppliers with NDC on PharmaCompass.
We have 13 companies offering Melphalan Hydrochloride
Get in contact with the supplier of your choice:
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