Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Ltd
02 1Aurobindo Pharma Limited
03 1Catalent Pharma Solutions, LLC
04 1Chromo Laboratories India Private Limited
05 1Cipla Ltd.
06 1Emcure Pharmaceuticals Limited
07 2Hetero Labs Limited
08 1Honour Lab Limited
09 1MSN Pharmachem Private Limited
10 2MYLAN LABORATORIES LIMITED
11 1Olon S.p.A.
12 1Raks Pharma Pvt. Limited
13 1SK BIOTEK IRELAND LIMITED
14 1SciAnda(Changshu) Pharmaceuticals, Ltd.
15 1Siegfried St. Vulbas SAS
16 1Tianish Laboratories Private Limited
01 4ATAZANAVIR SULFATE
02 1Atazanavir
03 11Atazanavir Sulfate
04 1Ataznavir Sulfate
05 1atazanavir sulfate
01 11India
02 1Italy
03 1Switzerland
04 1Taiwan
05 4U.S.A
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-005
Start Marketing Date : 2018-06-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : EXPORT ONLY
NDC Package Code : 11014-0175
Start Marketing Date : 2014-12-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50mg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 52562-008
Start Marketing Date : 2021-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7682
Start Marketing Date : 2016-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-806
Start Marketing Date : 2023-12-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50370-0049
Start Marketing Date : 2015-01-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0009
Start Marketing Date : 2012-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47621-050
Start Marketing Date : 2021-03-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54245-7031
Start Marketing Date : 2018-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50193-3264
Start Marketing Date : 2003-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Atazanavir Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Atazanavir Sulfate, including repackagers and relabelers. The FDA regulates Atazanavir Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Atazanavir Sulfate 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 Atazanavir Sulfate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Atazanavir Sulfate supplier is an individual or a company that provides Atazanavir Sulfate active pharmaceutical ingredient (API) or Atazanavir Sulfate finished formulations upon request. The Atazanavir Sulfate suppliers may include Atazanavir Sulfate API manufacturers, exporters, distributors and traders.
click here to find a list of Atazanavir Sulfate 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 Atazanavir Sulfate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Atazanavir Sulfate 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 Atazanavir Sulfate 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 Atazanavir Sulfate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Atazanavir Sulfate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Atazanavir Sulfate suppliers with NDC on PharmaCompass.
We have 16 companies offering Atazanavir Sulfate
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