Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Granules India Limited
03 1Bioindustria L.I.M. SpA
04 1DARMERICA, LLC
05 1MSN Organics Private Limited
06 1Pfizer Ireland Pharmaceuticals Unlimited Company
07 1Professional Compounding Centers of America dba PCCA
08 1n.v. Ajinomoto Omnichem S.A.
01 2PRAZOSIN HYDROCHLORIDE
02 1Prazosin HCl
03 4Prazosin Hydrochloride
04 1prazosin hydrochloride
01 3India
02 1Italy
03 1Japan
04 2U.S.A
05 1United Kingdom
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-043
Start Marketing Date : 2024-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-974
Start Marketing Date : 2021-04-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50923-0462
Start Marketing Date : 2009-10-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63809-2742
Start Marketing Date : 2003-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-132
Start Marketing Date : 2020-03-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50379-0019
Start Marketing Date : 2016-02-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-5040
Start Marketing Date : 2018-08-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 60715-0011
Start Marketing Date : 2020-09-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Prazosin Hydrochloride 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 Prazosin Hydrochloride manufacturer or Prazosin Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Prazosin Hydrochloride manufacturer or Prazosin Hydrochloride supplier.
PharmaCompass also assists you with knowing the Prazosin Hydrochloride API Price utilized in the formulation of products. Prazosin Hydrochloride API Price is not always fixed or binding as the Prazosin Hydrochloride Price is obtained through a variety of data sources. The Prazosin Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Minipress Xl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Minipress Xl, including repackagers and relabelers. The FDA regulates Minipress Xl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Minipress 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 Minipress Xl manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Minipress Xl supplier is an individual or a company that provides Minipress Xl active pharmaceutical ingredient (API) or Minipress Xl finished formulations upon request. The Minipress Xl suppliers may include Minipress Xl API manufacturers, exporters, distributors and traders.
click here to find a list of Minipress 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 Minipress Xl as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Minipress 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 Minipress 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 Minipress Xl and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Minipress Xl NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Minipress Xl suppliers with NDC on PharmaCompass.
We have 8 companies offering Minipress Xl
Get in contact with the supplier of your choice:
