01 1Aurobindo Pharma Limited
02 1Hetero Drugs Limited
03 1MSN Laboratories Private Limited
04 1MYLAN LABORATORIES LIMITED
05 1Piramal Pharma Limited
06 1Unichem Laboratories Limited, India
07 1Viyash Life Sciences Private Limited
08 1Zydus Lifesciences Limited
01 1PRAMIPEXOLE DIHYDROCHLORIDE MONOHYDRATE
02 1Pramipexole DiHydrochloride
03 4Pramipexole Dihydrochloride
04 2Pramipexole Dihydrochloride Monohydrate
01 6India
02 2U.S.A
NDC Package Code : 65862-506
Start Marketing Date : 2024-01-11
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0021
Start Marketing Date : 1997-07-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0052
Start Marketing Date : 2011-09-22
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65085-0056
Start Marketing Date : 2016-05-18
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-038
Start Marketing Date : 2012-03-31
End Marketing Date : 2026-12-31
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 : 82245-0120
Start Marketing Date : 1997-07-01
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65841-153
Start Marketing Date : 2018-01-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
96
PharmaCompass offers a list of Pramipexole Dihydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Pramipexole Dihydrochloride manufacturer or Pramipexole Dihydrochloride supplier for your needs.
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A Pramipexole Dihydrochloride Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pramipexole Dihydrochloride Monohydrate, including repackagers and relabelers. The FDA regulates Pramipexole Dihydrochloride Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pramipexole Dihydrochloride Monohydrate 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 Pramipexole Dihydrochloride Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Pramipexole Dihydrochloride Monohydrate supplier is an individual or a company that provides Pramipexole Dihydrochloride Monohydrate active pharmaceutical ingredient (API) or Pramipexole Dihydrochloride Monohydrate finished formulations upon request. The Pramipexole Dihydrochloride Monohydrate suppliers may include Pramipexole Dihydrochloride Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Pramipexole Dihydrochloride Monohydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Pramipexole Dihydrochloride Monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Pramipexole Dihydrochloride Monohydrate 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 Pramipexole Dihydrochloride Monohydrate 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 Pramipexole Dihydrochloride Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Pramipexole Dihydrochloride Monohydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Pramipexole Dihydrochloride Monohydrate suppliers with NDC on PharmaCompass.
We have 8 companies offering Pramipexole Dihydrochloride Monohydrate
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