Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1Aarti Pharmalabs Limited
02 1Arch Pharmalabs Limited
03 1DARMERICA, LLC
04 1Glenmark Life Sciences Limited
05 1Maithri Drugs Private Limited
06 1Medichem S.A.
07 1Olon S.p.A.
08 1Olon SpA
09 1QINGDAO TIDA BIOTEK CO.,LTD
10 1Shaoxing Hongming Pharmaceutical Technology Co., Ltd.
01 2ADAPALENE
02 1ADAPALENE MICRONIZED
03 7Adapalene
01 1China
02 4India
03 2Italy
04 1Spain
05 1U.S.A
06 1Blank
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
NDC Package Code : 15308-0716
Start Marketing Date : 1997-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-801
Start Marketing Date : 2005-09-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22365-120
Start Marketing Date : 2006-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (4kg/4kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71052-556
Start Marketing Date : 2019-07-30
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53296-0068
Start Marketing Date : 2010-05-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70600-047
Start Marketing Date : 2023-10-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0006
Start Marketing Date : 2016-03-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0100
Start Marketing Date : 2021-10-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 90027-010
Start Marketing Date : 2021-01-23
End Marketing Date : 2026-11-04
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 85169-001
Start Marketing Date : 2025-01-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Adapalene API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Adapalene manufacturer or Adapalene supplier for your needs.
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A Differin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Differin, including repackagers and relabelers. The FDA regulates Differin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Differin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Differin supplier is an individual or a company that provides Differin active pharmaceutical ingredient (API) or Differin finished formulations upon request. The Differin suppliers may include Differin API manufacturers, exporters, distributors and traders.
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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 Differin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Differin 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 Differin 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 Differin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Differin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Differin suppliers with NDC on PharmaCompass.
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