01 2BSV BioScience GmbH
02 1DARMERICA, LLC
03 1Qingdao Kangyuan Pharmaceutical Co., Ltd.
01 4Urofollitropin
01 1China
02 2Germany
03 1U.S.A
NDC Package Code : 76403-5001
Start Marketing Date : 2017-12-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1000000[iU]/1000000[iU])
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 76403-5002
Start Marketing Date : 2017-12-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (2000000[iU]/2000000[iU])
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 71052-066
Start Marketing Date : 2019-08-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100000U/100000U)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42205-0524
Start Marketing Date : 2019-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1000000U/1000000U)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Urofollitropin API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Urofollitropin manufacturer or Urofollitropin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Urofollitropin manufacturer or Urofollitropin supplier.
PharmaCompass also assists you with knowing the Urofollitropin API Price utilized in the formulation of products. Urofollitropin API Price is not always fixed or binding as the Urofollitropin Price is obtained through a variety of data sources. The Urofollitropin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fertinex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fertinex, including repackagers and relabelers. The FDA regulates Fertinex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fertinex API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fertinex supplier is an individual or a company that provides Fertinex active pharmaceutical ingredient (API) or Fertinex finished formulations upon request. The Fertinex suppliers may include Fertinex API manufacturers, exporters, distributors and traders.
click here to find a list of Fertinex 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 Fertinex as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fertinex 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 Fertinex 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 Fertinex and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fertinex NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fertinex suppliers with NDC on PharmaCompass.
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