With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 2USV Private Limited
03 2Anonima Materie Sintetiche and Affini (AMSA) Spa
04 1Cambrex Profarmaco Milano Srl
05 1KREATIVE ACTIVES PRIVATE LIMITED
06 1KREATIVE ORGANICS PRIVATE LIMITED
07 1Medisca Inc.
08 1Olon SpA
09 2Professional Compounding Centers of America
10 1Spectrum Laboratory Products, Inc.
11 1Sri Krishna Pharmaceuticals Ltd. Unit I
12 1Unichem Laboratories Limited, India
13 1Unique Chemicals
14 1Urquima, S.A.
01 4GLIPIZIDE
02 11Glipizide
03 2glipizide
01 1Finland
02 7India
03 3Italy
04 1Spain
05 3U.S.A
06 2United Kingdom
With Fermion, start the journey of your innovative API.
NDC Package Code : 12780-4680
Start Marketing Date : 2000-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
NDC Package Code : 62147-0001
Start Marketing Date : 2009-09-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
NDC Package Code : 62147-0400
Start Marketing Date : 2009-08-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17373-0161
Start Marketing Date : 2017-01-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17373-1060
Start Marketing Date : 2017-01-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12828-0051
Start Marketing Date : 1993-01-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48589-0008
Start Marketing Date : 2021-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0765
Start Marketing Date : 2015-08-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17337-0230
Start Marketing Date : 2010-11-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3299
Start Marketing Date : 1998-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Glipizide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glipizide, including repackagers and relabelers. The FDA regulates Glipizide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glipizide 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 Glipizide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glipizide supplier is an individual or a company that provides Glipizide active pharmaceutical ingredient (API) or Glipizide finished formulations upon request. The Glipizide suppliers may include Glipizide API manufacturers, exporters, distributors and traders.
click here to find a list of Glipizide 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 Glipizide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glipizide 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 Glipizide 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 Glipizide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glipizide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glipizide suppliers with NDC on PharmaCompass.
We have 13 companies offering Glipizide
Get in contact with the supplier of your choice:
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