01 1BIOCON LIMITED
02 1Biocon limited
03 1DARMERICA, LLC
04 1Divi's Laboratories Limited
05 1Formosa Laboratories, Inc.
06 1Shandong New Time Pharmaceutical Co., Ltd.
07 1Shanghai Tongming Biotechnology Co., Ltd.
01 1ORLISTST
02 5Orlistat
03 1Orlistat pellets
01 1China
02 3India
03 1Taiwan
04 1U.S.A
05 1Blank
NDC Package Code : 65727-015
Start Marketing Date : 2014-09-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65727-093
Start Marketing Date : 2024-03-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-110
Start Marketing Date : 2020-07-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (500g/500g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62331-045
Start Marketing Date : 2008-04-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66499-0043
Start Marketing Date : 2010-01-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42677-119
Start Marketing Date : 2022-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84143-002
Start Marketing Date : 2024-03-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Orlistat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Orlistat, including repackagers and relabelers. The FDA regulates Orlistat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Orlistat 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 Orlistat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Orlistat supplier is an individual or a company that provides Orlistat active pharmaceutical ingredient (API) or Orlistat finished formulations upon request. The Orlistat suppliers may include Orlistat API manufacturers, exporters, distributors and traders.
click here to find a list of Orlistat 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 Orlistat as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Orlistat 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 Orlistat 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 Orlistat and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Orlistat NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Orlistat suppliers with NDC on PharmaCompass.
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