Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1ADVANCED COMPOUNDS INTERNATIONAL, INC.
03 1Anthem Biosciences Pvt.Ltd.
04 1Cerbios-Pharma SA
05 1Essential Actives Corporation
06 1MOLCLONE LABS PRIVATE LIMITED
07 1Optimus Drugs Private Limited
08 1Professional Compounding Centers of America dba PCCA
01 15-METHYLTETRAHYDROFOLIC ACID
02 1L-5-MTHF
03 4LEVOMEFOLATE CALCIUM
04 2Levomefolate Calcium
01 4India
02 1Switzerland
03 2U.S.A
04 1United Kingdom
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-062
Start Marketing Date : 2020-03-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43615-002
Start Marketing Date : 2015-05-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76438-005
Start Marketing Date : 2021-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 54239-008
Start Marketing Date : 2012-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 80680-001
Start Marketing Date : 2020-09-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69723-002
Start Marketing Date : 2015-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-017
Start Marketing Date : 2019-12-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5180
Start Marketing Date : 2022-05-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Levomefolate Calcium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Levomefolate Calcium, including repackagers and relabelers. The FDA regulates Levomefolate Calcium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Levomefolate Calcium 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 Levomefolate Calcium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Levomefolate Calcium supplier is an individual or a company that provides Levomefolate Calcium active pharmaceutical ingredient (API) or Levomefolate Calcium finished formulations upon request. The Levomefolate Calcium suppliers may include Levomefolate Calcium API manufacturers, exporters, distributors and traders.
click here to find a list of Levomefolate Calcium 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 Levomefolate Calcium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Levomefolate Calcium 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 Levomefolate Calcium 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 Levomefolate Calcium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Levomefolate Calcium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Levomefolate Calcium suppliers with NDC on PharmaCompass.
We have 8 companies offering Levomefolate Calcium
Get in contact with the supplier of your choice:
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