Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
01 1METROCHEM API PRIVATE LIMITED
02 1Zhejiang Bamboo Pharmaceuticals Co.,Ltd
01 1LOXOPROFEN SODIUM HYDRATE
02 1Loxoprofen sodium
01 1China
02 1India
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
NDC Package Code : 42765-041
Start Marketing Date : 2021-07-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 81999-0010
Start Marketing Date : 2021-07-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Loxoprofen Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Loxoprofen Sodium, including repackagers and relabelers. The FDA regulates Loxoprofen Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Loxoprofen 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.
click here to find a list of Loxoprofen Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Loxoprofen Sodium supplier is an individual or a company that provides Loxoprofen Sodium active pharmaceutical ingredient (API) or Loxoprofen Sodium finished formulations upon request. The Loxoprofen Sodium suppliers may include Loxoprofen Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Loxoprofen Sodium 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 Loxoprofen Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Loxoprofen 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 Loxoprofen 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 Loxoprofen Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Loxoprofen Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Loxoprofen Sodium suppliers with NDC on PharmaCompass.
We have 2 companies offering Loxoprofen Sodium
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