Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
01 1Medichem Manufacturing (Malta) Ltd.
02 1Medichem S.A.
03 1Cadila Pharmaceuticals Limited
04 1HETERO DRUGS LIMITED
05 1HIKAL LIMITED
06 1Hubei Haosun Pharmaceutical Co., Ltd.
07 2MSN Life Sciences Private Limited
08 2MYLAN LABORATORIES LIMITED
09 1Pfizer Asia Manufacturing Pte Ltd
10 1R.L.Fine Chem Private Limited
11 1TAPI Croatia Industries Ltd.
12 1Tianish Laboratories Private Limited
13 1Zydus Lifesciences Limited
01 1DESVENLAFAXINE SUCCINATE
02 1DESVENLAFAXINE SUCCINATE MONOHYDRATE
03 1Desvenlafaxine
04 6Desvenlafaxine Succinate
05 2O-DESMETHYL VENLAFAXINE FUMARATE
06 1O-DESMETHYL VENLAFAXINE SUCCINATE
07 1O-Desmethyl Venlafaxine Succinate
08 1desvenlafaxine succinate
09 1o-desvenlafaxine succinate
01 1China
02 8India
03 2Spain
04 3U.S.A
05 1Blank
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
NDC Package Code : 16436-0087
Start Marketing Date : 2010-06-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
NDC Package Code : 53296-0087
Start Marketing Date : 2010-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65691-0067
Start Marketing Date : 2009-01-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0142
Start Marketing Date : 2014-08-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66651-928
Start Marketing Date : 2022-08-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14778-0606
Start Marketing Date : 2021-06-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-813
Start Marketing Date : 2015-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-723
Start Marketing Date : 2015-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65841-173
Start Marketing Date : 2018-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11722-023
Start Marketing Date : 2017-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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A Pristiq manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pristiq, including repackagers and relabelers. The FDA regulates Pristiq manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pristiq 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 Pristiq manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pristiq supplier is an individual or a company that provides Pristiq active pharmaceutical ingredient (API) or Pristiq finished formulations upon request. The Pristiq suppliers may include Pristiq API manufacturers, exporters, distributors and traders.
click here to find a list of Pristiq 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 Pristiq as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pristiq 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 Pristiq 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 Pristiq and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pristiq NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pristiq suppliers with NDC on PharmaCompass.
We have 11 companies offering Pristiq
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