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01 2Moehs Catalana SL

02 2Aurobindo Pharma Limited

03 1Chromo Laboratories India Private Limited

04 2Divi's Laboratories Limited

05 1Dr. Reddy┐s Laboratories Ltd.

06 1F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.

07 1Hunan Jiudian Pharmaceutical Co.,Ltd.

08 2MSN Pharmachem Private Limited

09 2Matrix Pharmacorp Private Limited

10 1Quimica Sintetica S.A.

11 2SMS Pharmaceuticals Limited

12 1SUN PHARMACEUTICAL INDUSTRIES, INC.

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMoehs Group, a reference company in the production of pharmaceutical active ingredients.

SUMATRIPTAN SUCCINATE

NDC Package Code : 52932-0727

Start Marketing Date : 2009-10-28

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

Moehs Iberica

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothMoehs Group, a reference company in the production of pharmaceutical active ingredients.

SUMATRIPTAN

NDC Package Code : 52932-0733

Start Marketing Date : 2009-10-28

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

Moehs Iberica

03

Bioprocess International Europe
Not Confirmed
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Bioprocess International Europe
Not Confirmed

SUMATRIPTAN SUCCINATE

NDC Package Code : 59651-151

Start Marketing Date : 2024-01-16

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (50kg/50kg)

Marketing Category : BULK INGREDIENT

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04

BPI Europe
Not Confirmed
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05

Bioprocess International Europe
Not Confirmed
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Bioprocess International Europe
Not Confirmed

SUMATRIPTAN SUCCINATE

NDC Package Code : 48087-0075

Start Marketing Date : 2010-04-09

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

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06

BPI Europe
Not Confirmed
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BPI Europe
Not Confirmed

SUMATRIPTAN SUCCINATE

NDC Package Code : 49574-517

Start Marketing Date : 2019-06-01

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

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07

Bioprocess International Europe
Not Confirmed
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Bioprocess International Europe
Not Confirmed

SUMATRIPTAN SUCCINATE

NDC Package Code : 50370-0014

Start Marketing Date : 2010-04-15

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

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08

Bioprocess International Europe
Not Confirmed
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Bioprocess International Europe
Not Confirmed

SUMATRIPTAN

NDC Package Code : 50370-0029

Start Marketing Date : 2011-12-29

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

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09

BPI Europe
Not Confirmed
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BPI Europe
Not Confirmed

SUMATRIPTAN SUCCINATE

NDC Package Code : 53069-0560

Start Marketing Date : 2000-04-05

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT

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10

Dr. Reddy┐s Laboratories Ltd.

Country
BPI Europe
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Dr. Reddy┐s Laboratories Ltd.

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BPI Europe
Not Confirmed

SUMATRIPTAN SUCCINATE

NDC Package Code : 55111-060

Start Marketing Date : 2003-03-21

End Marketing Date : 2026-12-31

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

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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Looking for 103628-46-2 / Sumatriptan API manufacturers, exporters & distributors?

Sumatriptan manufacturers, exporters & distributors 1

42

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

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

API | Excipient name

Sumatriptan

Synonyms

103628-46-2, Sumatran, Sumax, Imigran, Imitrex, Sumatriptanum

Cas Number

103628-46-2

Unique Ingredient Identifier (UNII)

8R78F6L9VO

About Sumatriptan

A serotonin agonist that acts selectively at 5HT1 receptors. It is used in the treatment of MIGRAINE DISORDERS.

Boots Pharmacy Migraine Relief Manufacturers

A Boots Pharmacy Migraine Relief manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Boots Pharmacy Migraine Relief, including repackagers and relabelers. The FDA regulates Boots Pharmacy Migraine Relief manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Boots Pharmacy Migraine Relief API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

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Boots Pharmacy Migraine Relief Suppliers

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

click here to find a list of Boots Pharmacy Migraine Relief suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.

Boots Pharmacy Migraine Relief 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 Boots Pharmacy Migraine Relief as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Boots Pharmacy Migraine Relief 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 Boots Pharmacy Migraine Relief 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 Boots Pharmacy Migraine Relief and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Boots Pharmacy Migraine Relief NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Boots Pharmacy Migraine Relief suppliers with NDC on PharmaCompass.

Boots Pharmacy Migraine Relief Manufacturers | Traders | Suppliers

Boots Pharmacy Migraine Relief 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.