01 1Alivira Animal Health Limited
01 1Imidocarb Dipropionate
01 1India
NDC Package Code : 86055-0023
Start Marketing Date : 2021-04-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Imidocarb Dipropionate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imidocarb Dipropionate, including repackagers and relabelers. The FDA regulates Imidocarb Dipropionate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imidocarb Dipropionate 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 Imidocarb Dipropionate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Imidocarb Dipropionate supplier is an individual or a company that provides Imidocarb Dipropionate active pharmaceutical ingredient (API) or Imidocarb Dipropionate finished formulations upon request. The Imidocarb Dipropionate suppliers may include Imidocarb Dipropionate API manufacturers, exporters, distributors and traders.
click here to find a list of Imidocarb Dipropionate 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 Imidocarb Dipropionate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Imidocarb Dipropionate 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 Imidocarb Dipropionate 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 Imidocarb Dipropionate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Imidocarb Dipropionate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Imidocarb Dipropionate suppliers with NDC on PharmaCompass.
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