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01 1Dr. Reddy's Laboratories Limited

02 1Dr.Reddy's laboratories Limited

03 1Aurobindo Pharma Limited

04 2Divi's Laboratories Limited

05 1Hetero Labs Limited

06 1LETCO MEDICAL, LLC

07 1Spectrum Laboratory Products, Inc.

08 2Zhejiang Charioteer Pharmaceutical Co., Ltd.

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

NAPROXEN SODIUM

NDC Package Code : 30007-815

Start Marketing Date : 2012-02-06

End Marketing Date : 2026-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

NAPROXEN SODIUM

NDC Package Code : 55111-004

Start Marketing Date : 1997-01-28

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

03

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

NAPROXEN SODIUM

NDC Package Code : 65862-507

Start Marketing Date : 2024-01-09

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (50kg/50kg)

Marketing Category : BULK INGREDIENT

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04

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

NAPROXEN SODIUM

NDC Package Code : 63310-2070

Start Marketing Date : 2005-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

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05

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

NAPROXEN SODIUM

NDC Package Code : 63310-2100

Start Marketing Date : 2012-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : DRUG FOR FURTHER PROCESSING

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06

AACR Annual meeting
Not Confirmed
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07

AACR Annual meeting
Not Confirmed
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08

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

NAPROXEN SODIUM

NDC Package Code : 68554-0129

Start Marketing Date : 1994-11-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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09

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

NAPROXEN SODIUM

NDC Package Code : 62991-2904

Start Marketing Date : 2010-11-23

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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10

AACR Annual meeting
Not Confirmed
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AACR Annual meeting
Not Confirmed

NAPROXEN SODIUM

NDC Package Code : 49452-4817

Start Marketing Date : 1994-12-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1g/g)

Marketing Category : BULK INGREDIENT

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Looking for 26159-34-2 / Naproxen Sodium API manufacturers, exporters & distributors?

Naproxen Sodium manufacturers, exporters & distributors 1

48

PharmaCompass offers a list of Naproxen Sodium 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 Naproxen Sodium manufacturer or Naproxen Sodium supplier for your needs.

Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Naproxen Sodium manufacturer or Naproxen Sodium supplier.

PharmaCompass also assists you with knowing the Naproxen Sodium API Price utilized in the formulation of products. Naproxen Sodium API Price is not always fixed or binding as the Naproxen Sodium Price is obtained through a variety of data sources. The Naproxen Sodium Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

API | Excipient name

Naproxen Sodium

Synonyms

26159-34-2, Naprelan, Anaprox, Naproxen sodium salt, Miranax, (-)-naproxen sodium

Cas Number

26159-34-2

Unique Ingredient Identifier (UNII)

9TN87S3A3C

About Naproxen Sodium

An anti-inflammatory agent with analgesic and antipyretic properties. Both the acid and its sodium salt are used in the treatment of rheumatoid arthritis and other rheumatic or musculoskeletal disorders, dysmenorrhea, and acute gout.

Flogen Manufacturers

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

Flogen Suppliers

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

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

Flogen 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 Flogen as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Flogen 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 Flogen 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 Flogen and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Flogen NDC to their finished compounded human drug products, they may choose to do so.

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

Flogen Manufacturers | Traders | Suppliers

Flogen Manufacturers, Traders, Suppliers 1
17

We have 7 companies offering Flogen

Get in contact with the supplier of your choice:

  1. Dr. Reddy's Laboratories
  2. Aurobindo Pharma Limited
  3. Charioteer
  4. Divis Laboratories
  5. Hetero Drugs
  6. Letco Medical
  7. Spectrum Chemical
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.