01 1Uquifa Spain
01 1Sodium Sulfachlorpyridazine
01 1Spain
NDC Package Code : 49711-1501
Start Marketing Date : 2009-10-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Sulfachlorpyridazine Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sulfachlorpyridazine Sodium, including repackagers and relabelers. The FDA regulates Sulfachlorpyridazine Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sulfachlorpyridazine Sodium 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 Sulfachlorpyridazine Sodium supplier is an individual or a company that provides Sulfachlorpyridazine Sodium active pharmaceutical ingredient (API) or Sulfachlorpyridazine Sodium finished formulations upon request. The Sulfachlorpyridazine Sodium suppliers may include Sulfachlorpyridazine Sodium 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 Sulfachlorpyridazine Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sulfachlorpyridazine Sodium 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 Sulfachlorpyridazine Sodium 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 Sulfachlorpyridazine Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sulfachlorpyridazine Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sulfachlorpyridazine Sodium suppliers with NDC on PharmaCompass.
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