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01 2Aurobindo Pharma Limited

02 1MATRIX LABORATORIES LIMITED

03 1MYLAN LABORATORIES LIMITED

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PharmaCompass

01

Pharmex
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Pharmex
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STAVUDINE

NDC Package Code : 65862-263

Start Marketing Date : 2024-01-16

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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02

Pharmex
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STAVUDINE

NDC Package Code : 65862-342

Start Marketing Date : 2024-01-16

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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03

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STAVUDINE

NDC Package Code : 65015-672

Start Marketing Date : 2015-01-12

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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04

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STAVUDINE

NDC Package Code : 65015-795

Start Marketing Date : 2011-05-27

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 3056-17-5 / Stavudine API manufacturers, exporters & distributors?

Stavudine manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Stavudine

Synonyms

3056-17-5, Sanilvudine, Zerit, 2',3'-didehydro-3'-deoxythymidine, Stavudinum, Zerit xr

Cas Number

3056-17-5

Unique Ingredient Identifier (UNII)

BO9LE4QFZF

About Stavudine

A dideoxynucleoside analog that inhibits reverse transcriptase and has in vitro activity against HIV.

Tox21_300583 Manufacturers

A Tox21_300583 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tox21_300583, including repackagers and relabelers. The FDA regulates Tox21_300583 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tox21_300583 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 Tox21_300583 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Tox21_300583 Suppliers

A Tox21_300583 supplier is an individual or a company that provides Tox21_300583 active pharmaceutical ingredient (API) or Tox21_300583 finished formulations upon request. The Tox21_300583 suppliers may include Tox21_300583 API manufacturers, exporters, distributors and traders.

click here to find a list of Tox21_300583 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Tox21_300583 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 Tox21_300583 as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Tox21_300583 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 Tox21_300583 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 Tox21_300583 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tox21_300583 NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Tox21_300583 suppliers with NDC on PharmaCompass.

Tox21_300583 Manufacturers | Traders | Suppliers

Tox21_300583 Manufacturers, Traders, Suppliers 1
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We have 2 companies offering Tox21_300583

Get in contact with the supplier of your choice:

  1. Aurobindo Pharma Limited
  2. Viatris
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.