ASolution Pharmaceuticals: Your Partner for cGMP Development & Manufacturing Services – Supplying APIs, FDFs, and Specialty Molecules.
01 1ASolution Pharmaceutical Private Limited
02 1ASolution Pharmaceuticals Private Limited
03 1NURAY CHEMICALS PRIVATE LIMITED
04 1Nuray Chemicals Private Limited
05 2Arch Pharmalabs Limited
06 1DARMERICA, LLC
07 2Derivados Quimicos
08 12F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
09 3Maithri Drugs Private Limited
10 1Micro Labs Limited
11 1Professional Compounding Centers of America
12 1Professional Compounding Centers of America dba PCCA
13 1TYCHE INDUSTRIES LIMITED
01 9NITROFURANTOIN
02 6NITROFURANTOIN MONOHYDRATE
03 1Nitrofurantoin
04 1Nitrofurantoin Anhydrous
05 1Nitrofurantoin Anhydrous (Macrocrystals)
06 1Nitrofurantoin Hydrous
07 1Nitrofurantoin Macrocrystal
08 3Nitrofurantoin Macrocrystals
09 5Nitrofurantoin Monohydrate
01 11India
02 12Italy
03 2Spain
04 1U.S.A
05 2United Kingdom
ASolution Pharmaceuticals: Your Partner for cGMP Development & Manufacturing Services – Supplying APIs, FDFs, and Specialty Molecules.
NDC Package Code : 84668-015
Start Marketing Date : 2024-08-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-038
Start Marketing Date : 2020-08-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
ASolution Pharmaceuticals: Your Partner for cGMP Development & Manufacturing Services – Supplying APIs, FDFs, and Specialty Molecules.
NDC Package Code : 84668-016
Start Marketing Date : 2024-08-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-045
Start Marketing Date : 2016-07-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22365-123
Start Marketing Date : 2003-04-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22365-122
Start Marketing Date : 2001-07-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0009
Start Marketing Date : 2010-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0026
Start Marketing Date : 2010-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 48087-0029
Start Marketing Date : 2010-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42571-396
Start Marketing Date : 2022-07-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
A Nitrofurantoin Monohydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nitrofurantoin Monohydrate, including repackagers and relabelers. The FDA regulates Nitrofurantoin Monohydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nitrofurantoin 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 Nitrofurantoin Monohydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nitrofurantoin Monohydrate supplier is an individual or a company that provides Nitrofurantoin Monohydrate active pharmaceutical ingredient (API) or Nitrofurantoin Monohydrate finished formulations upon request. The Nitrofurantoin Monohydrate suppliers may include Nitrofurantoin Monohydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Nitrofurantoin Monohydrate 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 Nitrofurantoin Monohydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nitrofurantoin 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 Nitrofurantoin 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 Nitrofurantoin Monohydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nitrofurantoin Monohydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nitrofurantoin Monohydrate suppliers with NDC on PharmaCompass.
We have 10 companies offering Nitrofurantoin Monohydrate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
