Minakem is manufacturing small molecules APIs including corticosteroids
01 2DELMAR CHEMICALS INC
02 1Fagron Inc
03 1Harman Finochem Limited
04 1LETCO MEDICAL, LLC
05 1Medisca Inc.
06 1SOLARA ACTIVE PHARMA SCIENCES LIMITED
07 1Spectrum Laboratory Products, Inc.
01 1SUCCINYLCHOLINE CHLORIDE
02 4Succinylcholine Chloride
03 3Succinylcholine Chloride Dihydrate
01 2Canada
02 2India
03 1Netherlands
04 3U.S.A
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-830
Start Marketing Date : 2006-08-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Minakem is manufacturing small molecules APIs including corticosteroids
NDC Package Code : 11712-832
Start Marketing Date : 2006-08-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SUCCINYLCHOLINE CHLORIDE DIHYDRATE
NDC Package Code : 51552-1611
Start Marketing Date : 2021-06-25
End Marketing Date : 2025-02-28
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 66064-1028
Start Marketing Date : 2017-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1262
Start Marketing Date : 2012-06-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
SUCCINYLCHOLINE CHLORIDE DIHYDRATE
NDC Package Code : 38779-1636
Start Marketing Date : 2016-01-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 72643-002
Start Marketing Date : 2011-12-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-7395
Start Marketing Date : 1995-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Suxamethonium Chloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Suxamethonium Chloride, including repackagers and relabelers. The FDA regulates Suxamethonium Chloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Suxamethonium Chloride 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 Suxamethonium Chloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Suxamethonium Chloride supplier is an individual or a company that provides Suxamethonium Chloride active pharmaceutical ingredient (API) or Suxamethonium Chloride finished formulations upon request. The Suxamethonium Chloride suppliers may include Suxamethonium Chloride API manufacturers, exporters, distributors and traders.
click here to find a list of Suxamethonium Chloride 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 Suxamethonium Chloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Suxamethonium Chloride 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 Suxamethonium Chloride 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 Suxamethonium Chloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Suxamethonium Chloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Suxamethonium Chloride suppliers with NDC on PharmaCompass.
We have 7 companies offering Suxamethonium Chloride
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