EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
01 1CHINOIN Pharmaceutical and Chemical Works Private Co. Ltd.
02 1EUROAPI Hungary Ltd.
03 1Fermion Oy
04 1SCI Pharmtech, Inc.
05 1AX Pharmaceutical Corp
06 1Chongqing Kangle Pharmaceutical Co., Ltd.
07 1DARMERICA, LLC
08 1Dasami Lab Private Limited
09 1HETERO LABS LIMITED
10 3Ipca Laboratories Limited
11 1MSN Life Sciences Private Limited
12 1Professional Compounding Centers of America
13 1SMS Pharmaceuticals Limited
14 1Spectrum Laboratory Products, Inc.
15 1Symed Labs Limited
16 1Zydus Lifesciences Limited
01 2HYDROXYCHLOROQUINE SULFATE
02 1Hydroxy Chloroquine Sulfate
03 1Hydroxy chloroquine Sulfate
04 12Hydroxychloroquine Sulfate
05 1Hydroxychloroquine sulfate
06 1hydroxychloroquine sulfate
01 1Canada
02 1China
03 1Finland
04 2France
05 9India
06 1Taiwan
07 2U.S.A
08 1United Kingdom
NDC Package Code : 45542-1161
Start Marketing Date : 2018-08-31
End Marketing Date : 2026-05-09
Dosage Form (Strength) : POWDER (40kg/40kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12780-2771
Start Marketing Date : 2016-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
NDC Package Code : 68108-0336
Start Marketing Date : 2012-12-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82231-108
Start Marketing Date : 2018-08-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1118
Start Marketing Date : 2012-02-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1220
Start Marketing Date : 2022-04-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-0198
Start Marketing Date : 2012-02-24
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0279
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-3625
Start Marketing Date : 1997-10-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65841-103
Start Marketing Date : 2017-09-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Hydroxychloroquine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Hydroxychloroquine, including repackagers and relabelers. The FDA regulates Hydroxychloroquine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Hydroxychloroquine 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 Hydroxychloroquine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Hydroxychloroquine supplier is an individual or a company that provides Hydroxychloroquine active pharmaceutical ingredient (API) or Hydroxychloroquine finished formulations upon request. The Hydroxychloroquine suppliers may include Hydroxychloroquine API manufacturers, exporters, distributors and traders.
click here to find a list of Hydroxychloroquine 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 Hydroxychloroquine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Hydroxychloroquine 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 Hydroxychloroquine 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 Hydroxychloroquine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Hydroxychloroquine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Hydroxychloroquine suppliers with NDC on PharmaCompass.
We have 15 companies offering Hydroxychloroquine
Get in contact with the supplier of your choice:
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