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01 1Ajinomoto OmniChem N.V.

02 1Aurobindo Pharma Limited

03 1Chromo Laboratories India Private Limited

04 1Glaxo Wellcome Manufacturing Pte. Ltd

05 1HETERO LABS LIMITED

06 1Hetero Labs Limited

07 1Honour Lab Limited

08 1MSN Life Sciences Private Limited

09 1Shanghai Desano Chemical Pharmaceutical Co., Ltd.

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11 2Tianish Laboratories Private Limited

12 1Viyash Life Sciences Private Limited

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PharmaCompass

01

The Generic Rx Session
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DOLUTEGRAVIR SODIUM

NDC Package Code : 50923-0116

Start Marketing Date : 2016-02-01

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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02

The Generic Rx Session
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The Generic Rx Session
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DOLUTEGRAVIR SODIUM

NDC Package Code : 65862-962

Start Marketing Date : 2023-11-02

End Marketing Date : 2024-12-31

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

Marketing Category : BULK INGREDIENT

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03

The Generic Rx Session
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04

The Generic Rx Session
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05

The Generic Rx Session
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The Generic Rx Session
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DOLUTEGRAVIR SODIUM

NDC Package Code : 68554-0093

Start Marketing Date : 2013-08-12

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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06

The Generic Rx Session
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The Generic Rx Session
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DOLUTEGRAVIR SODIUM

NDC Package Code : 68554-0135

Start Marketing Date : 2016-06-09

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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07

The Generic Rx Session
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The Generic Rx Session
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DOLUTEGRAVIR SODIUM

NDC Package Code : 69037-0044

Start Marketing Date : 2016-06-09

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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09

The Generic Rx Session
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DOLUTEGRAVIR SODIUM

NDC Package Code : 42931-242

Start Marketing Date : 2021-09-27

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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10

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DOLUTEGRAVIR SODIUM

NDC Package Code : 53044-001

Start Marketing Date : 2016-06-09

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 1051375-16-6 / Dolutegravir Sodium API manufacturers, exporters & distributors?

Dolutegravir Sodium manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Dolutegravir Sodium

Synonyms

1051375-16-6, Gsk1349572, S/gsk1349572, Tivicay, Gsk-1349572, Gsk 1349572

Cas Number

1051375-16-6

Unique Ingredient Identifier (UNII)

DKO1W9H7M1

About Dolutegravir Sodium

Dolutegravir is an orally bioavailable integrase strand-transfer inhibitor (INSTI), with activity against human immunodeficiency virus type 1 (HIV-1) infection. Upon oral administration, dolutegravir binds to the active site of integrase, an HIV enzyme that catalyzes the transfer of viral genetic material into human chromosomes. This prevents integrase from binding to retroviral deoxyribonucleic acid (DNA), and blocks the strand transfer step, which is essential for the HIV replication cycle. This prevents HIV-1 replication.

Dolutegravir / rilpivirine Manufacturers

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

Dolutegravir / rilpivirine Suppliers

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

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

Dolutegravir / rilpivirine 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 Dolutegravir / rilpivirine as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of Dolutegravir / rilpivirine suppliers with NDC on PharmaCompass.

Dolutegravir / rilpivirine Manufacturers | Traders | Suppliers

Dolutegravir / rilpivirine 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.