01 1AURORIUM LLC
02 4Adare Pharmaceuticals Inc
03 1Adare Pharmaceuticls, Inc.
04 1Glenmark Life Sciences Limited
05 1Global Calcium Private Limited
06 1Herbamed AG
07 1K+S Minerals and Agriculture GmbH
08 1Klinge Chemicals Ltd
09 1Laboratoire Schmidt-Nagel Inc.
10 1Macco Organiques Inc
11 1Macco Organiques, S.R.O.
12 1Maithri Drugs Private Limited
13 1Professional Compounding Centers of America dba PCCA
14 2Spectrum Laboratory Products, Inc.
15 1THINQ Pharma-CRO Limited
01 1Aconitum napellus, Gelsemium sempervirens, Ipecacaunha, Pulsatilla nigrans, Bryonia alba, Chamomilla, Allium cepa, Euphrasia officinalis, Sambucus nigra, Echinacea angustifolia
02 1Kali muriaticum 12C, Prunus spinosa 30C, Silicea 30C, Sarsaparilla 30C
03 3POTASSIUM CHLORIDE
04 12Potassium Chloride
05 1Potassium chloride
06 1potassium chloride
01 2Canada
02 2Germany
03 3India
04 1Switzerland
05 8U.S.A
06 2United Kingdom
07 1Blank
NDC Package Code : 59917-054
Start Marketing Date : 1985-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.87kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 59917-055
Start Marketing Date : 1985-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (0.87kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 11951-1839
Start Marketing Date : 2017-11-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 30092-022
Start Marketing Date : 2001-10-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51933-1100
Start Marketing Date : 1980-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55897-004
Start Marketing Date : 2024-04-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5061
Start Marketing Date : 2019-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-5780
Start Marketing Date : 1990-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-5770
Start Marketing Date : 1989-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54469-0008
Start Marketing Date : 2023-08-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
14
PharmaCompass offers a list of Potassium Chloride 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 Potassium Chloride manufacturer or Potassium Chloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Potassium Chloride manufacturer or Potassium Chloride supplier.
PharmaCompass also assists you with knowing the Potassium Chloride API Price utilized in the formulation of products. Potassium Chloride API Price is not always fixed or binding as the Potassium Chloride Price is obtained through a variety of data sources. The Potassium Chloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 05433_FLUKA manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 05433_FLUKA, including repackagers and relabelers. The FDA regulates 05433_FLUKA manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 05433_FLUKA 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 05433_FLUKA manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 05433_FLUKA supplier is an individual or a company that provides 05433_FLUKA active pharmaceutical ingredient (API) or 05433_FLUKA finished formulations upon request. The 05433_FLUKA suppliers may include 05433_FLUKA API manufacturers, exporters, distributors and traders.
click here to find a list of 05433_FLUKA 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 05433_FLUKA as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for 05433_FLUKA 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 05433_FLUKA 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 05433_FLUKA and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 05433_FLUKA NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of 05433_FLUKA suppliers with NDC on PharmaCompass.
We have 12 companies offering 05433_FLUKA
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