01 1RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA
02 1Shanghai Wonder Pharmaceutical Co. Ltd.
03 1Spectrum Laboratory Products, Inc.
01 1DIMENHYDRINATE
02 2Dimenhydrinate
01 1China
02 1Italy
03 1U.S.A
NDC Package Code : 12711-4675
Start Marketing Date : 1982-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 55745-0002
Start Marketing Date : 2016-08-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-2615
Start Marketing Date : 1993-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Dimenhydrinate 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 Dimenhydrinate manufacturer or Dimenhydrinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dimenhydrinate manufacturer or Dimenhydrinate supplier.
PharmaCompass also assists you with knowing the Dimenhydrinate API Price utilized in the formulation of products. Dimenhydrinate API Price is not always fixed or binding as the Dimenhydrinate Price is obtained through a variety of data sources. The Dimenhydrinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Vomisin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vomisin, including repackagers and relabelers. The FDA regulates Vomisin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vomisin 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 Vomisin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Vomisin supplier is an individual or a company that provides Vomisin active pharmaceutical ingredient (API) or Vomisin finished formulations upon request. The Vomisin suppliers may include Vomisin API manufacturers, exporters, distributors and traders.
click here to find a list of Vomisin 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 Vomisin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Vomisin 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 Vomisin 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 Vomisin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Vomisin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Vomisin suppliers with NDC on PharmaCompass.
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