Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
01 1Chunghwa Chemical Synthesis & Biotech. Ltd
02 1Biocon Limited
03 1CKD Bio Corporation
04 4Concord Biotech Limited
05 1DARMERICA, LLC
06 1Dasami Lab Private Limited
07 1Emcure Pharmaceuticals Limited
08 1Excella GmbH & Co. KG
09 1Formosa Laboratories, Inc.
10 1Hisun Pharmaceutical (Hangzhou) Co., Ltd.
11 1Novartis Pharmaceuticals Corporation
12 1Professional Compounding Centers of America
13 1TAPI Czech Industries s.r.o.
14 1TEVA Czech Industries s.r.o
15 1Wuxi Fortune Pharmaceutical Co.,Ltd.
01 4MYCOPHENOLATE MOFETIL
02 12Mycophenolate Mofetil
03 1Mycophenolate Mofetile
04 1mycophenolate mofetil
01 2China
02 7India
03 1Israel
04 1Luxembourg
05 1South Korea
06 1Switzerland
07 2Taiwan
08 1U.S.A
09 1United Kingdom
10 1Blank
Chunghwa provides cost-effective APIs & advanced intermediates with complete DMF or COS, ensuring quality & reliable production.
NDC Package Code : 52076-6220
Start Marketing Date : 2018-01-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65727-005
Start Marketing Date : 2004-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52972-0037
Start Marketing Date : 2011-06-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-876
Start Marketing Date : 2023-09-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (6kg/6kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46014-1123
Start Marketing Date : 2007-12-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51187-0003
Start Marketing Date : 2019-09-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0078-1385
Start Marketing Date : 2008-10-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5125
Start Marketing Date : 2020-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 47848-019
Start Marketing Date : 2021-05-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65050-2101
Start Marketing Date : 2021-01-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
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PharmaCompass offers a list of Mycophenolate Mofetil 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 Mycophenolate Mofetil manufacturer or Mycophenolate Mofetil supplier for your needs.
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PharmaCompass also assists you with knowing the Mycophenolate Mofetil API Price utilized in the formulation of products. Mycophenolate Mofetil API Price is not always fixed or binding as the Mycophenolate Mofetil Price is obtained through a variety of data sources. The Mycophenolate Mofetil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Mycophenolate mofetil Teva manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Mycophenolate mofetil Teva, including repackagers and relabelers. The FDA regulates Mycophenolate mofetil Teva manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Mycophenolate mofetil Teva API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Mycophenolate mofetil Teva supplier is an individual or a company that provides Mycophenolate mofetil Teva active pharmaceutical ingredient (API) or Mycophenolate mofetil Teva finished formulations upon request. The Mycophenolate mofetil Teva suppliers may include Mycophenolate mofetil Teva API manufacturers, exporters, distributors and traders.
click here to find a list of Mycophenolate mofetil Teva 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 Mycophenolate mofetil Teva as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Mycophenolate mofetil Teva 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 Mycophenolate mofetil Teva 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 Mycophenolate mofetil Teva and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Mycophenolate mofetil Teva NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Mycophenolate mofetil Teva suppliers with NDC on PharmaCompass.
We have 14 companies offering Mycophenolate mofetil Teva
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