USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
01 1USV Private Limited
02 1Aurobindo Pharma Limited
03 1Cadila Pharmaceuticals Limited
04 1Cambrex Profarmaco Milano Srl
05 2Dipharma Francis Srl
01 5Glyburide
02 1Glyburide Micronized
01 3India
02 2Italy
03 1U.S.A
USV offers custom peptide synthesis ranging from gram to multi-gram to multi-kilogram quantities.
NDC Package Code : 62147-0002
Start Marketing Date : 2009-09-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-318
Start Marketing Date : 2023-11-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65691-0041
Start Marketing Date : 2004-01-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0066
Start Marketing Date : 1993-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0059
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 : 46438-0064
Start Marketing Date : 2012-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Glibenclamide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glibenclamide, including repackagers and relabelers. The FDA regulates Glibenclamide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glibenclamide 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 Glibenclamide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glibenclamide supplier is an individual or a company that provides Glibenclamide active pharmaceutical ingredient (API) or Glibenclamide finished formulations upon request. The Glibenclamide suppliers may include Glibenclamide API manufacturers, exporters, distributors and traders.
click here to find a list of Glibenclamide 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 Glibenclamide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glibenclamide 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 Glibenclamide 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 Glibenclamide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glibenclamide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glibenclamide suppliers with NDC on PharmaCompass.
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