01 2Aurobindo Pharma Limited
02 1MATRIX LABORATORIES LIMITED
03 1MYLAN LABORATORIES LIMITED
01 2STAVUDINE
02 2Stavudine
01 2India
02 2U.S.A
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
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
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
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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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.
A C07312 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of C07312, including repackagers and relabelers. The FDA regulates C07312 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. C07312 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 C07312 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A C07312 supplier is an individual or a company that provides C07312 active pharmaceutical ingredient (API) or C07312 finished formulations upon request. The C07312 suppliers may include C07312 API manufacturers, exporters, distributors and traders.
click here to find a list of C07312 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 C07312 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for C07312 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 C07312 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 C07312 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a C07312 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of C07312 suppliers with NDC on PharmaCompass.
We have 2 companies offering C07312
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