Veranova: A CDMO that manages complexity with confidence.
01 1MACFARLAN SMITH LIMITED
02 2FRANCOPIA
03 2Sanofi Winthrop Industrie
04 1Fagron Services BV
05 1LETCO MEDICAL, LLC
06 2Medisca Inc.
07 1Professional Compounding Centers of America dba PCCA
08 1Spectrum Laboratory Products, Inc.
01 6APOMORPHINE HYDROCHLORIDE
02 1Apomorphine HCl
03 4Apomorphine Hydrochloride
01 4France
02 1Netherlands
03 5U.S.A
04 1United Kingdom
Veranova: A CDMO that manages complexity with confidence.
NDC Package Code : 12707-031
Start Marketing Date : 2017-12-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-6007
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 50396-6009
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 52465-104
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 52465-105
Start Marketing Date : 2014-06-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1513
Start Marketing Date : 2010-10-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-1764
Start Marketing Date : 2014-07-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-3276
Start Marketing Date : 2022-10-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-2303
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-0700
Start Marketing Date : 2005-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Apomorphine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Apomorphine Hydrochloride, including repackagers and relabelers. The FDA regulates Apomorphine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Apomorphine Hydrochloride 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 Apomorphine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Apomorphine Hydrochloride supplier is an individual or a company that provides Apomorphine Hydrochloride active pharmaceutical ingredient (API) or Apomorphine Hydrochloride finished formulations upon request. The Apomorphine Hydrochloride suppliers may include Apomorphine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Apomorphine Hydrochloride 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 Apomorphine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Apomorphine Hydrochloride 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 Apomorphine Hydrochloride 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 Apomorphine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Apomorphine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Apomorphine Hydrochloride suppliers with NDC on PharmaCompass.
We have 7 companies offering Apomorphine Hydrochloride
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