01 2AMCOL Health & Beauty Solutions, Inc DBA AMCOL Household and Personal Care
02 1AMCOL Health & Beauty Solutions, Inc. DBA
03 1Asclemed USA Inc.
04 1Chongqing Huapont Pharmaceutical Co Ltd
05 1DARMERICA, LLC
06 1Fagron Inc
07 1Galenova Inc
08 1Genvion Corporation
09 1KALCHEM INTERNATIONAL INC.
10 1LETCO MEDICAL, LLC
11 1Medisca Inc.
12 2Olon SpA
13 1Professional Compounding Centers of America dba PCCA
14 1Siegfried PharmaChemikalien Minden GmbH
15 1Sionc Pharmaceutical Private Limited
16 1Spectrum Laboratory Products, Inc.
01 5TRETINOIN
02 12Tretinoin
03 1Tretinoin M
01 2Canada
02 1China
03 1India
04 2Italy
05 1Netherlands
06 1Switzerland
07 9U.S.A
08 1United Kingdom
NDC Package Code : 48943-0011
Start Marketing Date : 2000-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0120
Start Marketing Date : 1998-04-01
End Marketing Date : 2025-04-15
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 62049-003
Start Marketing Date : 2015-07-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60592-738
Start Marketing Date : 2023-10-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-2057
Start Marketing Date : 2011-11-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0001
Start Marketing Date : 2015-07-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 17337-0036
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0045
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-1270
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-6243
Start Marketing Date : 1995-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Tretinoin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tretinoin, including repackagers and relabelers. The FDA regulates Tretinoin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tretinoin 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 Tretinoin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tretinoin supplier is an individual or a company that provides Tretinoin active pharmaceutical ingredient (API) or Tretinoin finished formulations upon request. The Tretinoin suppliers may include Tretinoin API manufacturers, exporters, distributors and traders.
click here to find a list of Tretinoin 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 Tretinoin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tretinoin 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 Tretinoin 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 Tretinoin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tretinoin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tretinoin suppliers with NDC on PharmaCompass.
We have 15 companies offering Tretinoin
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