Inke S.A: APIs manufacturing plant.
01 1Inke SA
02 1Coral Drugs Private Limited
03 1VAMSI LABS LIMITED.
04 1Farmabios S.p.A.
05 1Fermion Oy
06 2Amphastar Nanjing Pharmaceuticals, Inc.
07 1Cipla Ltd.
08 3Industriale Chimica s.r.l.
09 2Lusochimica SPA
10 1MSN Laboratories Private Limited
11 1MYLAN LABORATORIES LIMITED
12 1Medisca Inc.
13 1Professional Compounding Centers of America
14 3Sicor S.r.l.
15 1Viyash Life Sciences Private Limited
01 1FORMOTEROL FUMARATE
02 2FORMOTEROL FUMARATE DIHYDRATE
03 6Formoterol Fumarate
04 8Formoterol Fumarate Dihydrate
05 1Formoterol Fumarate Dihydrate CR
06 1Formoterol Fumarate Dihydrate MC
07 1Formoterol fumarate
08 1formoterol fumarate
01 1Finland
02 1Germany
03 5India
04 8Italy
05 1Spain
06 4U.S.A
07 1United Kingdom
Inke S.A: APIs manufacturing plant.
NDC Package Code : 64567-0006
Start Marketing Date : 2008-06-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Coral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.
NDC Package Code : 49076-7001
Start Marketing Date : 2016-02-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Vamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.
NDC Package Code : 66412-0204
Start Marketing Date : 2023-09-25
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
Axplora- The partner of choice for complex APIs.
NDC Package Code : 46439-8763
Start Marketing Date : 2018-06-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
With Fermion, start the journey of your innovative API.
NDC Package Code : 12780-4880
Start Marketing Date : 2016-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43898-0130
Start Marketing Date : 2010-05-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43898-0131
Start Marketing Date : 2010-05-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-2295
Start Marketing Date : 2022-03-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0087
Start Marketing Date : 2014-02-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0216
Start Marketing Date : 2021-10-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Formoterol Fumarate Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Formoterol Fumarate Dihydrate, including repackagers and relabelers. The FDA regulates Formoterol Fumarate Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Formoterol Fumarate Dihydrate 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 Formoterol Fumarate Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Formoterol Fumarate Dihydrate supplier is an individual or a company that provides Formoterol Fumarate Dihydrate active pharmaceutical ingredient (API) or Formoterol Fumarate Dihydrate finished formulations upon request. The Formoterol Fumarate Dihydrate suppliers may include Formoterol Fumarate Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Formoterol Fumarate Dihydrate 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 Formoterol Fumarate Dihydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Formoterol Fumarate Dihydrate 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 Formoterol Fumarate Dihydrate 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 Formoterol Fumarate Dihydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Formoterol Fumarate Dihydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Formoterol Fumarate Dihydrate suppliers with NDC on PharmaCompass.
We have 15 companies offering Formoterol Fumarate Dihydrate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
