Neuland Laboratories- A dedicated 100% API provider.
01 1Neuland Laboratories Limited
01 1ROPINIROLE
01 1India
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-1011
Start Marketing Date : 2015-09-12
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 Ropinirole 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 Ropinirole manufacturer or Ropinirole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Ropinirole manufacturer or Ropinirole supplier.
PharmaCompass also assists you with knowing the Ropinirole API Price utilized in the formulation of products. Ropinirole API Price is not always fixed or binding as the Ropinirole Price is obtained through a variety of data sources. The Ropinirole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A ReQuip XL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ReQuip XL, including repackagers and relabelers. The FDA regulates ReQuip XL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ReQuip XL 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 ReQuip XL manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A ReQuip XL supplier is an individual or a company that provides ReQuip XL active pharmaceutical ingredient (API) or ReQuip XL finished formulations upon request. The ReQuip XL suppliers may include ReQuip XL API manufacturers, exporters, distributors and traders.
click here to find a list of ReQuip XL 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 ReQuip XL as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ReQuip XL 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 ReQuip XL 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 ReQuip XL and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ReQuip XL NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ReQuip XL suppliers with NDC on PharmaCompass.
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