01 1Brichem Sciences Private Limited
02 1SCH Global Services Private Limited
01 2Nandrolone Phenylpropionate
01 2Blank
NDC Package Code : 85207-042
Start Marketing Date : 2026-03-02
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 87456-005
Start Marketing Date : 2026-03-02
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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PharmaCompass offers a list of Nandrolone Phenpropionate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Nandrolone Phenpropionate manufacturer or Nandrolone Phenpropionate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Nandrolone Phenpropionate manufacturer or Nandrolone Phenpropionate supplier.
A Equibolin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Equibolin, including repackagers and relabelers. The FDA regulates Equibolin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Equibolin 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 Equibolin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Equibolin supplier is an individual or a company that provides Equibolin active pharmaceutical ingredient (API) or Equibolin finished formulations upon request. The Equibolin suppliers may include Equibolin API manufacturers, exporters, distributors and traders.
click here to find a list of Equibolin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Equibolin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Equibolin 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 Equibolin 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 Equibolin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Equibolin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Equibolin suppliers with NDC on PharmaCompass.
