01 1Dipharma Francis Srl
02 1LETCO MEDICAL, LLC
03 2Olon S.p.A.
04 1Professional Compounding Centers of America
05 1Professional Compounding Centers of America dba PCCA
06 1R.L.Fine Chem Private Limited
07 1Sigma-Aldrich Ireland Ltd.
08 1Spectrum Laboratory Products, Inc.
09 1Vasudha Pharma Chem Limited
01 2NORTRIPTYLINE HYDROCHLORIDE
02 8Nortriptyline Hydrochloride
01 2India
02 3Italy
03 3U.S.A
04 2United Kingdom
NDC Package Code : 46438-0049
Start Marketing Date : 2012-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2905
Start Marketing Date : 2010-12-09
End Marketing Date : 2027-02-28
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0547
Start Marketing Date : 2024-09-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0534
Start Marketing Date : 2020-03-03
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER ()
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-2175
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 : 51927-0128
Start Marketing Date : 2021-06-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 71554-011
Start Marketing Date : 2019-04-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54154-007
Start Marketing Date : 2010-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4858
Start Marketing Date : 1997-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66577-025
Start Marketing Date : 1984-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Nortriptyline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nortriptyline, including repackagers and relabelers. The FDA regulates Nortriptyline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nortriptyline 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 Nortriptyline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nortriptyline supplier is an individual or a company that provides Nortriptyline active pharmaceutical ingredient (API) or Nortriptyline finished formulations upon request. The Nortriptyline suppliers may include Nortriptyline API manufacturers, exporters, distributors and traders.
click here to find a list of Nortriptyline 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 Nortriptyline as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nortriptyline 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 Nortriptyline 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 Nortriptyline and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nortriptyline NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nortriptyline suppliers with NDC on PharmaCompass.
We have 8 companies offering Nortriptyline
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