Axplora- The partner of choice for complex APIs.
01 1PharmaZell GmbH
02 1Medichem S.A.
03 2Industriale Chimica s.r.l.
04 1Jubilant Pharmova Limited
05 2PROCOS S.p.A.
06 2Quimica Sintetica S.A.
07 1Unichem Laboratories Limited, India
01 3GUANFACINE HYDROCHLORIDE
02 1GUANFACINEHYDROCHLORIDE
03 1Guanfacine
04 4Guanfacine Hydrochloride
05 1Guanfacine Hydrochloride Micronized
01 1Germany
02 2India
03 4Italy
04 3Spain
Axplora- The partner of choice for complex APIs.
NDC Package Code : 12598-9508
Start Marketing Date : 2014-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Medichem is a vertically integrated pharmaceutical company specializing in the development & manufacturing of APIs & FDFs.
NDC Package Code : 53296-0024
Start Marketing Date : 2010-03-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0250
Start Marketing Date : 2008-12-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63190-0390
Start Marketing Date : 2008-12-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1177
Start Marketing Date : 2014-03-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46016-2912
Start Marketing Date : 2013-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46016-2911
Start Marketing Date : 2022-03-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53069-1150
Start Marketing Date : 2024-09-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53069-0080
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-096
Start Marketing Date : 2020-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Guanfacine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Guanfacine, including repackagers and relabelers. The FDA regulates Guanfacine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Guanfacine 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 Guanfacine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Guanfacine supplier is an individual or a company that provides Guanfacine active pharmaceutical ingredient (API) or Guanfacine finished formulations upon request. The Guanfacine suppliers may include Guanfacine API manufacturers, exporters, distributors and traders.
click here to find a list of Guanfacine 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 Guanfacine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Guanfacine 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 Guanfacine 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 Guanfacine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Guanfacine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Guanfacine suppliers with NDC on PharmaCompass.
We have 7 companies offering Guanfacine
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