Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Limited
02 1AURORIUM LLC
03 4Adare Pharmaceuticals Inc
04 1Adare Pharmaceuticls, Inc.
05 1Glenmark Life Sciences Limited
06 1Global Calcium Private Limited
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 1Professional Compounding Centers of America dba PCCA
13 2Spectrum Laboratory Products, Inc.
14 1THINQ Pharma-CRO Limited
01 1Aconitum napellus, Gelsemium sempervirens, Ipecacaunha, Pulsatilla nigrans, Bryonia alba, Chamomilla, Allium cepa, Euphrasia officinalis, Sambucus nigra, Echinacea angustifolia
02 3POTASSIUM CHLORIDE
03 11Potassium Chloride
04 2Potassium chloride
05 1potassium chloride
01 2Canada
02 1Germany
03 4India
04 1Switzerland
05 8U.S.A
06 2United Kingdom
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-725
Start Marketing Date : 2021-05-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : EXPORT ONLY
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 : 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
A K-Dur manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of K-Dur, including repackagers and relabelers. The FDA regulates K-Dur manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. K-Dur 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 K-Dur manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A K-Dur supplier is an individual or a company that provides K-Dur active pharmaceutical ingredient (API) or K-Dur finished formulations upon request. The K-Dur suppliers may include K-Dur API manufacturers, exporters, distributors and traders.
click here to find a list of K-Dur 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 K-Dur as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for K-Dur 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 K-Dur 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 K-Dur and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a K-Dur NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of K-Dur suppliers with NDC on PharmaCompass.
We have 12 companies offering K-Dur
Get in contact with the supplier of your choice:
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