Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
01 2Interquim, S.A.
02 1Nuray Chemicals Private Limited
03 1Amino Chemicals Ltd
04 1Aurobindo Pharma Limited
05 1Cambrex Charles City, Inc
06 1Curia New York, Inc.
07 1Glenmark Life Sciences Limited
08 1MSN Life Sciences Private Limited
09 2Olon S.p.A.
10 1ScinoPharm Taiwan Ltd.
11 1Sicor de Mexico S.A. de C.V
01 12Lifitegrast
02 1Lifitegrast Type II
01 4India
02 2Italy
03 1Malta
04 1Mexico
05 2Spain
06 1Taiwan
07 2U.S.A
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
NDC Package Code : 64552-4088
Start Marketing Date : 2016-11-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-054
Start Marketing Date : 2017-10-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Interquim comes from an international group of 50 companies active in the pharma, hospital, diagnostics, fine chemicals & feed sectors.
NDC Package Code : 64552-4089
Start Marketing Date : 2016-11-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-445
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-5170
Start Marketing Date : 2017-08-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65392-2803
Start Marketing Date : 2016-07-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17337-0431
Start Marketing Date : 2021-05-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0433
Start Marketing Date : 2022-06-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65129-1428
Start Marketing Date : 2020-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63592-3385
Start Marketing Date : 2018-02-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Lifitegrast manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lifitegrast, including repackagers and relabelers. The FDA regulates Lifitegrast manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lifitegrast 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 Lifitegrast manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lifitegrast supplier is an individual or a company that provides Lifitegrast active pharmaceutical ingredient (API) or Lifitegrast finished formulations upon request. The Lifitegrast suppliers may include Lifitegrast API manufacturers, exporters, distributors and traders.
click here to find a list of Lifitegrast 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 Lifitegrast as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lifitegrast 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 Lifitegrast 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 Lifitegrast and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lifitegrast NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lifitegrast suppliers with NDC on PharmaCompass.
We have 11 companies offering Lifitegrast
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