Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1NURAY CHEMICALS PRIVATE LIMITED
02 1Changzhou Tianhua Pharmaceutical Co., Ltd.
03 1Fagron Inc
04 1Galenova Inc
05 1LETCO MEDICAL, LLC
06 1Medisca Inc.
07 1Professional Compounding Centers of America
08 1Professional Compounding Centers of America dba PCCA
09 1Siegfried Evionnaz SA
10 1Spectrum Laboratory Products, Inc.
11 1Venkata Narayana Active Ingredients Private Limited
12 1W. R. GRACE & CO.-CONN.
01 1Lidocaine Tetracaine Hydrochloride
02 2TETRACAINE HYDROCHLORIDE
03 9Tetracaine Hydrochloride
01 1Canada
02 1China
03 2India
04 1Netherlands
05 1Switzerland
06 4U.S.A
07 2United Kingdom
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-108
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 : 51552-0269
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1mg/mg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 22568-1029
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2067
Start Marketing Date : 2012-07-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0566
Start Marketing Date : 2014-08-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0142
Start Marketing Date : 2021-06-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1241
Start Marketing Date : 2013-06-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17381-100
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 : 49452-7680
Start Marketing Date : 1990-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52038-004
Start Marketing Date : 2020-01-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Tetracaine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetracaine Hydrochloride, including repackagers and relabelers. The FDA regulates Tetracaine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetracaine Hydrochloride 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 Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetracaine Hydrochloride supplier is an individual or a company that provides Tetracaine Hydrochloride active pharmaceutical ingredient (API) or Tetracaine Hydrochloride finished formulations upon request. The Tetracaine Hydrochloride suppliers may include Tetracaine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tetracaine Hydrochloride 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 Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tetracaine Hydrochloride 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 Hydrochloride 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 Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tetracaine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tetracaine Hydrochloride suppliers with NDC on PharmaCompass.
We have 11 companies offering Tetracaine Hydrochloride
Get in contact with the supplier of your choice:
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