01 1DARMERICA, LLC
02 1Hangzhou Sinodo Pharm Technology Co.,Ltd
03 1Hangzhou XinHan Biopharma Co., Ltd.
04 1Qingdao Biopeptek Co., Ltd.
05 2Zhejiang Peptites Biotech
01 1IPAMORELIN Acetate
02 4Ipamorelin
03 1Ipamorelin Acetate
01 2China
02 2U.S.A
03 2Blank
NDC Package Code : 73212-006
Start Marketing Date : 2020-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-222
Start Marketing Date : 2019-09-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 73569-053
Start Marketing Date : 2024-08-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 73569-061
Start Marketing Date : 2024-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82907-476
Start Marketing Date : 2023-12-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (10g/10g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 84789-104
Start Marketing Date : 2024-09-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
A Ipamorelin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ipamorelin, including repackagers and relabelers. The FDA regulates Ipamorelin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ipamorelin 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 Ipamorelin supplier is an individual or a company that provides Ipamorelin active pharmaceutical ingredient (API) or Ipamorelin finished formulations upon request. The Ipamorelin suppliers may include Ipamorelin API manufacturers, exporters, distributors and traders.
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 Ipamorelin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ipamorelin 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 Ipamorelin 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 Ipamorelin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ipamorelin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ipamorelin suppliers with NDC on PharmaCompass.
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