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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

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

HYDROXYCHLOROQUINE SULFATE

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

EUROAPI Compnay Banner

02

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Cosmoprof
Not Confirmed
  • fda
  • EDQM
  • WHO-GMP

Virtual BoothWith Fermion, start the journey of your innovative API.

HYDROXYCHLOROQUINE SULFATE

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

fermion

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothSCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.

HYDROXYCHLOROQUINE SULFATE

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

SCI Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEUROAPI, the leading small molecules API player, provides both API sales & CDMO services.

HYDROXYCHLOROQUINE SULFATE

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

EUROAPI Compnay Banner

08

Cosmoprof
Not Confirmed
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Cosmoprof
Not Confirmed

HYDROXYCHLOROQUINE SULFATE

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...

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09

Cosmoprof
Not Confirmed
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10

Cosmoprof
Not Confirmed
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Cosmoprof
Not Confirmed

HYDROXYCHLOROQUINE SULFATE

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

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Plaquenil Manufacturers

A Plaquenil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Plaquenil, including repackagers and relabelers. The FDA regulates Plaquenil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Plaquenil 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 Plaquenil manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Plaquenil Suppliers

A Plaquenil supplier is an individual or a company that provides Plaquenil active pharmaceutical ingredient (API) or Plaquenil finished formulations upon request. The Plaquenil suppliers may include Plaquenil API manufacturers, exporters, distributors and traders.

click here to find a list of Plaquenil suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Plaquenil NDC

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 Plaquenil as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Plaquenil API and other APIs are published in this directory by the FDA.

Unfinished drugs

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 Plaquenil 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.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Plaquenil and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Plaquenil NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Plaquenil suppliers with NDC on PharmaCompass.

Plaquenil Manufacturers | Traders | Suppliers

Plaquenil Manufacturers, Traders, Suppliers 1
Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.