Aspen API. More than just an API.
01 1Aspen Oss B.V.
02 1Bachem Americas, Inc.
03 1Assia Chemical Industries Ltd - Teva Tech Site
04 1Aurobindo Pharma Limited
05 1BCN PEPTIDES SA
06 1Darmerica
07 1Hybio Pharmaceutical Co., Ltd.
08 17Piramal Pharma Limited
09 2PolyPeptide Laboratories (Sweden) AB
10 1Professional Compounding Centers of America
11 1ScinoPharm Taiwan Ltd.
01 1DESMOPRESSIN
02 19Desmopressin
03 6Desmopressin Acetate
04 2Desmopressin acetate
01 1China
02 1India
03 1Israel
04 1Netherlands
05 1Spain
06 3Switzerland
07 1Taiwan
08 18U.S.A
09 1United Kingdom
NDC Package Code : 60870-0440
Start Marketing Date : 1999-07-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Bachem Group is a public, innovation-driven company specializing in the development and manufacturing of peptides and oligonucleotides.
NDC Package Code : 52416-108
Start Marketing Date : 2001-09-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : EXPORT ONLY
NDC Package Code : 35207-0001
Start Marketing Date : 2015-05-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14403-0012
Start Marketing Date : 2022-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 41701-007
Start Marketing Date : 2011-03-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10g/10g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 41701-007
Start Marketing Date : 2011-03-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (115g/115g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 41701-007
Start Marketing Date : 2011-03-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (150g/150g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 41701-007
Start Marketing Date : 2011-03-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (80g/80g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 41701-007
Start Marketing Date : 2011-03-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (200g/200g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 41701-007
Start Marketing Date : 2011-03-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (85g/85g)
Marketing Category : BULK INGREDIENT
A Desmopressin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desmopressin, including repackagers and relabelers. The FDA regulates Desmopressin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desmopressin 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 Desmopressin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Desmopressin supplier is an individual or a company that provides Desmopressin active pharmaceutical ingredient (API) or Desmopressin finished formulations upon request. The Desmopressin suppliers may include Desmopressin API manufacturers, exporters, distributors and traders.
click here to find a list of Desmopressin 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 Desmopressin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Desmopressin 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 Desmopressin 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 Desmopressin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Desmopressin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Desmopressin suppliers with NDC on PharmaCompass.
We have 11 companies offering Desmopressin
Get in contact with the supplier of your choice:
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