Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
01 1Olpha AS
02 1Celgene Chemicals Sarl
03 1Hetero Labs Limited
04 1Micro-Macinazione SA
05 1Siegfried AG
06 1VALARY LAB PRIVATE LIMITED
01 4THALIDOMIDE
02 2Thalidomide
01 1India
02 1Latvia
03 2Switzerland
04 1U.S.A
05 1Blank
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
NDC Package Code : 63818-0424
Start Marketing Date : 2010-06-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82991-205
Start Marketing Date : 2007-11-19
End Marketing Date : 2027-05-27
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 68554-0011
Start Marketing Date : 1998-07-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10745-0543
Start Marketing Date : 2023-07-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17205-205
Start Marketing Date : 2023-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 81955-0015
Start Marketing Date : 1998-07-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Thalidomide 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 Thalidomide manufacturer or Thalidomide supplier for your needs.
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A Distoval manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Distoval, including repackagers and relabelers. The FDA regulates Distoval manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Distoval 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 Distoval supplier is an individual or a company that provides Distoval active pharmaceutical ingredient (API) or Distoval finished formulations upon request. The Distoval suppliers may include Distoval API manufacturers, exporters, distributors and traders.
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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 Distoval as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Distoval 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 Distoval 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 Distoval and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Distoval NDC to their finished compounded human drug products, they may choose to do so.
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