Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 1Symbiotec Pharmalab Private Limited
01 1Testosterone Phenylpropionate
01 1India
Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
NDC Package Code : 22552-0011
Start Marketing Date : 2010-04-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Testosterone Phenylpropionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Testosterone Phenylpropionate, including repackagers and relabelers. The FDA regulates Testosterone Phenylpropionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Testosterone Phenylpropionate 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 Testosterone Phenylpropionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Testosterone Phenylpropionate supplier is an individual or a company that provides Testosterone Phenylpropionate active pharmaceutical ingredient (API) or Testosterone Phenylpropionate finished formulations upon request. The Testosterone Phenylpropionate suppliers may include Testosterone Phenylpropionate API manufacturers, exporters, distributors and traders.
click here to find a list of Testosterone Phenylpropionate 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 Testosterone Phenylpropionate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Testosterone Phenylpropionate 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 Testosterone Phenylpropionate 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 Testosterone Phenylpropionate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Testosterone Phenylpropionate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Testosterone Phenylpropionate suppliers with NDC on PharmaCompass.
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