01 1Chieron Active Ingredients Private Limited
02 1Fagron Essentials, LLC
03 1Galenova Inc
04 1KALCHEM INTERNATIONAL INC
05 1LETCO MEDICAL, LLC
06 1Medisca Inc.
07 1Professional Compounding Centers of America
08 1Professional Compounding Centers of America dba PCCA
09 1Spectrum Laboratory Products, Inc.
10 1W. R. GRACE & CO.-CONN.
01 1Lidocaine Tetracaine Hydrochloride
02 1TETRACAINE HCL
03 3TETRACAINE HYDROCHLORIDE
04 5Tetracaine Hydrochloride
01 1Canada
02 1Netherlands
03 5U.S.A
04 2United Kingdom
05 1Blank
NDC Package Code : 51552-0269
Start Marketing Date : 1998-04-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1mg/mg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 79572-034
Start Marketing Date : 2021-05-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1029
Start Marketing Date : 2021-06-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-785
Start Marketing Date : 2025-10-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2067
Start Marketing Date : 2012-07-28
End Marketing Date : 2027-12-31
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 : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0374
Start Marketing Date : 2025-09-04
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1241
Start Marketing Date : 2013-06-20
End Marketing Date : 2029-01-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-7680
Start Marketing Date : 1990-06-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52038-004
Start Marketing Date : 2020-01-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Portfolio PDF
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PharmaCompass offers a list of Tetracaine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tetracaine Hydrochloride manufacturer or Tetracaine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetracaine Hydrochloride manufacturer or Tetracaine Hydrochloride supplier.
A Anacel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Anacel, including repackagers and relabelers. The FDA regulates Anacel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Anacel 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 Anacel manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Anacel supplier is an individual or a company that provides Anacel active pharmaceutical ingredient (API) or Anacel finished formulations upon request. The Anacel suppliers may include Anacel API manufacturers, exporters, distributors and traders.
click here to find a list of Anacel suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Anacel as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Anacel 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 Anacel 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 Anacel and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Anacel NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Anacel suppliers with NDC on PharmaCompass.
We have 8 companies offering Anacel
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