01 1Apicore US LLC
02 1DARMERICA, LLC
03 1TAPI Czech Industries s.r.o.
04 1Teva Czech Industries s.r.o
05 1YS Life Science Co., Ltd.
01 1CABERGOLINE
02 4Cabergoline
01 1India
02 1Israel
03 1South Korea
04 1U.S.A
05 1Blank
NDC Package Code : 14096-153
Start Marketing Date : 2013-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-018
Start Marketing Date : 2023-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47848-009
Start Marketing Date : 2017-12-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 40016-011
Start Marketing Date : 2020-04-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84644-009
Start Marketing Date : 2017-12-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
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A Cabergoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cabergoline, including repackagers and relabelers. The FDA regulates Cabergoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cabergoline 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 Cabergoline manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cabergoline supplier is an individual or a company that provides Cabergoline active pharmaceutical ingredient (API) or Cabergoline finished formulations upon request. The Cabergoline suppliers may include Cabergoline API manufacturers, exporters, distributors and traders.
click here to find a list of Cabergoline 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 Cabergoline as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cabergoline 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 Cabergoline 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 Cabergoline and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cabergoline NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cabergoline suppliers with NDC on PharmaCompass.
We have 4 companies offering Cabergoline
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