Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 2Alchem International Private Ltd
02 1Porton Pharma Solutions Ltd
03 1BGP healthcare private limited
04 10Cambrex Charles City, Inc
05 1Harman Finochem Limited
06 4Nicobrand LTD
07 1Professional Compounding Centers of America dba PCCA
08 2Siegfried AG
01 1NICOTINE BITARTRATE
02 2NICOTINE POLACRILEX
03 1Nicotine
04 1Nicotine Bitartrate Dihydrate
05 9Nicotine Polacrilex
06 7Nicotine Resinate
07 1nicotine tartrate
01 1China
02 4India
03 4Ireland
04 2Switzerland
05 10U.S.A
06 1United Kingdom
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
NDC Package Code : 55742-125
Start Marketing Date : 2014-08-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 75877-0002
Start Marketing Date : 2012-02-27
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 : 55742-128
Start Marketing Date : 2016-12-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50392-102
Start Marketing Date : 2015-06-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-1803
Start Marketing Date : 2016-04-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-1800
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-1801
Start Marketing Date : 2012-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-3406
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17205-105
Start Marketing Date : 2004-03-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17205-483
Start Marketing Date : 2012-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Nicotine Bitartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nicotine Bitartrate, including repackagers and relabelers. The FDA regulates Nicotine Bitartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nicotine Bitartrate 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 Nicotine Bitartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nicotine Bitartrate supplier is an individual or a company that provides Nicotine Bitartrate active pharmaceutical ingredient (API) or Nicotine Bitartrate finished formulations upon request. The Nicotine Bitartrate suppliers may include Nicotine Bitartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Nicotine Bitartrate 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 Nicotine Bitartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nicotine Bitartrate 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 Nicotine Bitartrate 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 Nicotine Bitartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nicotine Bitartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nicotine Bitartrate suppliers with NDC on PharmaCompass.
We have 8 companies offering Nicotine Bitartrate
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