01 1Aurobindo Pharma Limited
02 1Cipla Ltd.
03 1Curia Spain S.A.U.
04 1Erregierre SpA
05 1Hetero Drugs Limited
06 1MSN Laboratories Private Limited
07 1MYLAN LABORATORIES LIMITED
08 1Piramal Pharma Limited
09 1Unichem Laboratories Limited, India
10 1Viyash Life Sciences Private Limited
11 1Zydus Lifesciences Limited
01 1PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
02 1Pramipexole DiHydrochloride
03 7Pramipexole Dihydrochloride
04 2Pramipexole Dihydrochloride Monohydrate
01 7India
02 1Italy
03 3U.S.A
NDC Package Code : 65862-506
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7589
Start Marketing Date : 2016-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65089-0040
Start Marketing Date : 2010-02-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-1868
Start Marketing Date : 2010-07-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0021
Start Marketing Date : 1997-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0052
Start Marketing Date : 2011-09-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65085-0056
Start Marketing Date : 2016-05-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-038
Start Marketing Date : 2012-03-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-768
Start Marketing Date : 2015-02-19
End Marketing Date : 2026-12-01
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65841-153
Start Marketing Date : 2018-01-12
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 Pramipexole 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 Pramipexole manufacturer or Pramipexole supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Pramipexole manufacturer or Pramipexole supplier.
PharmaCompass also assists you with knowing the Pramipexole API Price utilized in the formulation of products. Pramipexole API Price is not always fixed or binding as the Pramipexole Price is obtained through a variety of data sources. The Pramipexole Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sifrol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sifrol, including repackagers and relabelers. The FDA regulates Sifrol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sifrol 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 Sifrol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sifrol supplier is an individual or a company that provides Sifrol active pharmaceutical ingredient (API) or Sifrol finished formulations upon request. The Sifrol suppliers may include Sifrol API manufacturers, exporters, distributors and traders.
click here to find a list of Sifrol 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 Sifrol as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Sifrol 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 Sifrol 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 Sifrol and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Sifrol NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Sifrol suppliers with NDC on PharmaCompass.
We have 11 companies offering Sifrol
Get in contact with the supplier of your choice:
