Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 2Alchem International Private Ltd
02 4Alps Pharmaceutical Ind. Co., Ltd.
03 1K PATEL PHYTO EXTRACTIONS PRIVATE LIMITED
04 8K. Patel Phyto Extractions Private Limited
05 1Kothari Phytochemicals International
06 1SAB HERBALS AND NUTRACEUTICALS
07 9SHASHI PHYTOCHEMICAL INDUSTRIES
01 5CALCIUM SENNOSIDES
02 9Calcium Sennosides
03 1Calcium Sennosides 20%
04 9SENNOSIDES
05 1Senna Dry Extract
06 1Sennosides
01 1Canada
02 21India
03 4Japan
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC Package Code : 55742-007
Start Marketing Date : 2012-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC Package Code : 55742-012
Start Marketing Date : 2012-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17353-0903
Start Marketing Date : 2011-08-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17353-0902
Start Marketing Date : 2013-09-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 17353-0903
Start Marketing Date : 2011-08-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17353-0903
Start Marketing Date : 2011-08-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52537-001
Start Marketing Date : 2012-12-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55977-100
Start Marketing Date : 1996-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55977-200
Start Marketing Date : 1996-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 55977-300
Start Marketing Date : 1996-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Sennosides manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sennosides, including repackagers and relabelers. The FDA regulates Sennosides manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sennosides 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 Sennosides manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sennosides supplier is an individual or a company that provides Sennosides active pharmaceutical ingredient (API) or Sennosides finished formulations upon request. The Sennosides suppliers may include Sennosides API manufacturers, exporters, distributors and traders.
click here to find a list of Sennosides 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 Sennosides as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sennosides 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 Sennosides 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 Sennosides and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sennosides NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sennosides suppliers with NDC on PharmaCompass.
We have 6 companies offering Sennosides
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