01 1Olon SpA
02 1Professional Compounding Centers of America dba PCCA
01 1PHENDIMETRAZINE TARTRATE
02 1Phendimetrazine Tartrate
01 1Italy
02 1United Kingdom
NDC Package Code : 17337-0029
Start Marketing Date : 2012-12-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5043
Start Marketing Date : 2018-09-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Phendimetrazine Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Phendimetrazine Tartrate, including repackagers and relabelers. The FDA regulates Phendimetrazine Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Phendimetrazine Tartrate 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 Phendimetrazine Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Phendimetrazine Tartrate supplier is an individual or a company that provides Phendimetrazine Tartrate active pharmaceutical ingredient (API) or Phendimetrazine Tartrate finished formulations upon request. The Phendimetrazine Tartrate suppliers may include Phendimetrazine Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Phendimetrazine Tartrate 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 Phendimetrazine Tartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Phendimetrazine Tartrate 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 Phendimetrazine Tartrate 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 Phendimetrazine Tartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Phendimetrazine Tartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Phendimetrazine Tartrate suppliers with NDC on PharmaCompass.
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