DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1DASAMI LAB PRIVATE LIMITED
03 2Lonza AG
04 1Siegfried Evionnaz SA
01 1LUMATEPERONE TOSYLATE
02 2Lumateperone Tosylate
03 1Lumateperone tosylate
04 1Lumateperone tosylate non mc
01 2India
02 1Switzerland
03 2U.S.A
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 71796-058
Start Marketing Date : 2023-03-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70966-0039
Start Marketing Date : 2019-12-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49187-0820
Start Marketing Date : 2019-07-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49187-0821
Start Marketing Date : 2019-07-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17381-803
Start Marketing Date : 2020-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Lumateperone Tosylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lumateperone Tosylate, including repackagers and relabelers. The FDA regulates Lumateperone Tosylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lumateperone Tosylate 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 Lumateperone Tosylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lumateperone Tosylate supplier is an individual or a company that provides Lumateperone Tosylate active pharmaceutical ingredient (API) or Lumateperone Tosylate finished formulations upon request. The Lumateperone Tosylate suppliers may include Lumateperone Tosylate API manufacturers, exporters, distributors and traders.
click here to find a list of Lumateperone Tosylate 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 Lumateperone Tosylate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lumateperone Tosylate 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 Lumateperone Tosylate 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 Lumateperone Tosylate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lumateperone Tosylate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lumateperone Tosylate suppliers with NDC on PharmaCompass.
We have 4 companies offering Lumateperone Tosylate
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