Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Operations GmbH
02 2AURORE PHARMACEUTICALS PRIVATE LIMITED
03 1Aurobindo Pharma Limited
04 1Cambrex Charles City, Inc.
05 1Cipla Ltd.
06 1Dasami Lab Private Limited
07 1Esteve Huayi Pharmaceuticals Co., Ltd
08 2Hetero Labs Limited
09 1Laurus Labs Limited
10 2MYLAN LABORATORIES LIMITED
11 1Macleods Pharmaceuticals Limited
12 1Mylan Laboratories Limited
13 2Tianish Laboratories Private Limited
14 1Uquifa Spain
15 1Yuhan Chemical Inc.
01 5EMTRICITABINE
02 10Emtricitabine
03 1Emtricitabine (Process -II)
04 1GS-9036
05 2emtricitabine
01 1China
02 1Germany
03 11India
04 1South Korea
05 1Spain
06 4U.S.A
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
NDC Package Code : 52696-0008
Start Marketing Date : 2007-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59116-7480
Start Marketing Date : 2014-09-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7637
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 : 59997-0005
Start Marketing Date : 2020-02-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42385-304
Start Marketing Date : 2010-04-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 33342-500
Start Marketing Date : 2015-11-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49711-1516
Start Marketing Date : 2013-02-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-883
Start Marketing Date : 2017-12-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-838
Start Marketing Date : 2013-10-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-827
Start Marketing Date : 2013-06-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Emtricitabine / Tenofovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emtricitabine / Tenofovir, including repackagers and relabelers. The FDA regulates Emtricitabine / Tenofovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emtricitabine / Tenofovir 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 Emtricitabine / Tenofovir manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Emtricitabine / Tenofovir supplier is an individual or a company that provides Emtricitabine / Tenofovir active pharmaceutical ingredient (API) or Emtricitabine / Tenofovir finished formulations upon request. The Emtricitabine / Tenofovir suppliers may include Emtricitabine / Tenofovir API manufacturers, exporters, distributors and traders.
click here to find a list of Emtricitabine / Tenofovir 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 Emtricitabine / Tenofovir as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Emtricitabine / Tenofovir 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 Emtricitabine / Tenofovir 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 Emtricitabine / Tenofovir and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Emtricitabine / Tenofovir NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Emtricitabine / Tenofovir suppliers with NDC on PharmaCompass.
We have 14 companies offering Emtricitabine / Tenofovir
Get in contact with the supplier of your choice:
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