EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1EUROAPI Germany GmbH
02 1CAMBREX PROFARMACO MILANO SRL
03 1Centaur Pharmaceuticals Private Limited
04 2F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
05 1Honour Lab Limited
06 1MSN Life Sciences Private Limited
07 1Micro Labs Limited
08 1Piramal Pharma Limited
09 1Raks Pharma Pvt. Limited
01 3CLOBAZAM
02 6Clobazam
03 1clobazam
01 1France
02 5India
03 2Italy
04 2U.S.A
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
NDC Package Code : 82348-103
Start Marketing Date : 2020-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0084
Start Marketing Date : 2016-07-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 64330-110
Start Marketing Date : 2015-02-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0094
Start Marketing Date : 2010-11-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0117
Start Marketing Date : 2015-01-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69037-0009
Start Marketing Date : 2011-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42571-308
Start Marketing Date : 2022-01-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69766-016
Start Marketing Date : 2016-08-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65085-0054
Start Marketing Date : 2018-12-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47621-047
Start Marketing Date : 2016-03-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Urbanol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Urbanol, including repackagers and relabelers. The FDA regulates Urbanol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Urbanol 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 Urbanol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Urbanol supplier is an individual or a company that provides Urbanol active pharmaceutical ingredient (API) or Urbanol finished formulations upon request. The Urbanol suppliers may include Urbanol API manufacturers, exporters, distributors and traders.
click here to find a list of Urbanol 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 Urbanol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Urbanol 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 Urbanol 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 Urbanol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Urbanol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Urbanol suppliers with NDC on PharmaCompass.
We have 9 companies offering Urbanol
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