01 1SYMBIOTICA SPECIALITY INGREDIENTS SDN.BHD
01 1CLOBETASONE BUTYRATE
01 1Malaysia
NDC Package Code : 52128-153
Start Marketing Date : 2013-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Clobetasone Butyrate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Clobetasone Butyrate manufacturer or Clobetasone Butyrate supplier for your needs.
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PharmaCompass also assists you with knowing the Clobetasone Butyrate API Price utilized in the formulation of products. Clobetasone Butyrate API Price is not always fixed or binding as the Clobetasone Butyrate Price is obtained through a variety of data sources. The Clobetasone Butyrate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Trimovate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimovate, including repackagers and relabelers. The FDA regulates Trimovate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimovate 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 Trimovate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimovate supplier is an individual or a company that provides Trimovate active pharmaceutical ingredient (API) or Trimovate finished formulations upon request. The Trimovate suppliers may include Trimovate API manufacturers, exporters, distributors and traders.
click here to find a list of Trimovate 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 Trimovate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Trimovate 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 Trimovate 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 Trimovate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Trimovate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Trimovate suppliers with NDC on PharmaCompass.
