China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
01 1Shandong Chenghui Shuangda Pharmaceutical Co., Ltd.
02 1NURAY CHEMICALS PRIVATE LIMITED
03 1Changzhou Tianhua Pharmaceutical Co., Ltd.
04 1Fagron Inc
05 1LETCO MEDICAL, LLC
06 1Medisca Inc.
07 1Professional Compounding Centers of America dba PCCA
08 1Siegfried Evionnaz SA
09 1Spectrum Laboratory Products, Inc.
10 1Venkata Narayana Active Ingredients Private Limited
01 1TETRACAINE
02 9Tetracaine
01 2China
02 2India
03 1Netherlands
04 1Switzerland
05 3U.S.A
06 1United Kingdom
China's leading API and intermediate manufacturer, offering CMO/CDMO services and exports to 70+ countries, enhancing global health.
NDC Package Code : 82481-004
Start Marketing Date : 2022-01-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-107
Start Marketing Date : 2024-10-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66219-0003
Start Marketing Date : 2009-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0323
Start Marketing Date : 2004-09-01
End Marketing Date : 2026-01-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62991-1708
Start Marketing Date : 2010-07-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0374
Start Marketing Date : 2014-06-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0007
Start Marketing Date : 2019-02-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17381-099
Start Marketing Date : 2010-05-18
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-7675
Start Marketing Date : 1991-10-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52038-001
Start Marketing Date : 2010-08-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Tetracaine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetracaine, including repackagers and relabelers. The FDA regulates Tetracaine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetracaine 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 Tetracaine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetracaine supplier is an individual or a company that provides Tetracaine active pharmaceutical ingredient (API) or Tetracaine finished formulations upon request. The Tetracaine suppliers may include Tetracaine API manufacturers, exporters, distributors and traders.
click here to find a list of Tetracaine 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 Tetracaine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tetracaine 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 Tetracaine 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 Tetracaine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tetracaine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tetracaine suppliers with NDC on PharmaCompass.
We have 10 companies offering Tetracaine
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