01 1AbbVie Inc.
02 1CKD Bio Corporation
03 2Concord Biotech Limited
04 3Curia Italy S.r.l.
05 1Curia Italy s.r.l
06 1Fujian Kerui Pharmaceutical Co., Ltd.
07 2Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd
08 1Joyang Laboratories
09 1LETCO MEDICAL, LLC
10 1Medisca Inc.
11 1North China Pharmaceutical Huasheng Co. Ltd.
12 1Novartis Ringaskiddy Limited
13 1PROFESSIONAL COMPOUNDING CENTERS OF AMERICA
14 1Professional Compounding Centers of America
15 1Sterling Pharma Solutions Limited
16 1TAPI Czech Industries s.r.o.
17 1Teva Czech Industries s.r.o
18 1Zhejiang Ruibang Laboratories
01 7CYCLOSPORINE
02 1CYCLOSPORINE A
03 1Ciclosporin
04 11Cyclosporine
05 1Cyclosporine A
06 1cyclosporin
01 6China
02 2India
03 1Israel
04 1South Korea
05 1Switzerland
06 7U.S.A
07 3United Kingdom
08 1Blank
NDC Package Code : 0074-5503
Start Marketing Date : 2010-05-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52972-0027
Start Marketing Date : 1996-11-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55486-1567
Start Marketing Date : 2012-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55486-1602
Start Marketing Date : 2012-06-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52928-005
Start Marketing Date : 2021-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0660
Start Marketing Date : 2014-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0213
Start Marketing Date : 2021-09-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0160
Start Marketing Date : 2003-08-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 50384-6300
Start Marketing Date : 2023-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (307kg/307kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-004
Start Marketing Date : 2022-01-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Cyclosporine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cyclosporine, including repackagers and relabelers. The FDA regulates Cyclosporine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cyclosporine 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 Cyclosporine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cyclosporine supplier is an individual or a company that provides Cyclosporine active pharmaceutical ingredient (API) or Cyclosporine finished formulations upon request. The Cyclosporine suppliers may include Cyclosporine API manufacturers, exporters, distributors and traders.
click here to find a list of Cyclosporine 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 Cyclosporine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cyclosporine 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 Cyclosporine 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 Cyclosporine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cyclosporine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cyclosporine suppliers with NDC on PharmaCompass.
We have 15 companies offering Cyclosporine
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