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01 1Coral Drugs Private Limited

02 1VAMSI LABS LIMITED.

03 1Farmabios S.p.A.

04 1Fermion Oy

05 2Amphastar Nanjing Pharmaceuticals, Inc.

06 1Cipla Ltd.

07 3Industriale Chimica s.r.l.

08 2Lusochimica SPA

09 1MSN Laboratories Private Limited

10 1MYLAN LABORATORIES LIMITED

11 1Medisca Inc.

12 1Professional Compounding Centers of America

13 3Sicor S.r.l.

14 1Viyash Life Sciences Private Limited

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCoral's API range includes Corticosteroids, Antihistamines. Hormones and Antineoplastics.

FORMOTEROL FUMARATE

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

Corel Drugs cGMP partner for APIs

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothVamsi Labs is one of the major manufacturers of Anti-asthmatic, Anti-migraine & Anti-psychotic APIs.

FORMOTEROL FUMARATE

NDC Package Code : 66412-0204

Start Marketing Date : 2023-09-25

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

Vamsi Labs

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAxplora is your partner of choice for complex APIs.

FORMOTEROL FUMARATE

NDC Package Code : 46439-8763

Start Marketing Date : 2018-06-20

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

Axplora CB

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWith Fermion, start the journey of your innovative API.

FORMOTEROL FUMARATE

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

fermion

05

Peptide Therapy Summit
Not Confirmed
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Peptide Therapy Summit
Not Confirmed

FORMOTEROL FUMARATE

NDC Package Code : 52221-116

Start Marketing Date : 2015-10-30

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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06

Peptide Therapy Summit
Not Confirmed
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Peptide Therapy Summit
Not Confirmed

FORMOTEROL FUMARATE

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

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07

Peptide Therapy Summit
Not Confirmed
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Peptide Therapy Summit
Not Confirmed

FORMOTEROL FUMARATE

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

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08

Peptide Therapy Summit
Not Confirmed
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Peptide Therapy Summit
Not Confirmed

FORMOTEROL FUMARATE

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

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09

Peptide Therapy Summit
Not Confirmed
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10

Peptide Therapy Summit
Not Confirmed
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Peptide Therapy Summit
Not Confirmed

FORMOTEROL FUMARATE

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...

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Looking for / Formoterol Fumarate API manufacturers, exporters & distributors?

Formoterol Fumarate manufacturers, exporters & distributors 1

50

PharmaCompass offers a list of Formoterol Fumarate 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 Formoterol Fumarate manufacturer or Formoterol Fumarate supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Formoterol Fumarate manufacturer or Formoterol Fumarate supplier.

PharmaCompass also assists you with knowing the Formoterol Fumarate API Price utilized in the formulation of products. Formoterol Fumarate API Price is not always fixed or binding as the Formoterol Fumarate Price is obtained through a variety of data sources. The Formoterol Fumarate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Formoterol Fumarate

Synonyms

Mls001401438, Chembl1895091, Hms2051p14, Hms2233m10, Ccg-101038, Nc00288

Dulera Manufacturers

A Dulera manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dulera, including repackagers and relabelers. The FDA regulates Dulera manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dulera 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 Dulera manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Dulera Suppliers

A Dulera supplier is an individual or a company that provides Dulera active pharmaceutical ingredient (API) or Dulera finished formulations upon request. The Dulera suppliers may include Dulera API manufacturers, exporters, distributors and traders.

click here to find a list of Dulera suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Dulera NDC

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 Dulera as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Dulera API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Dulera 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Dulera and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dulera NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Dulera suppliers with NDC on PharmaCompass.

Dulera Manufacturers | Traders | Suppliers

Dulera Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.