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PharmaCompass

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ETODOLAC

NDC Package Code : 17373-0186

Start Marketing Date : 2017-01-02

End Marketing Date : 2024-12-31

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

Marketing Category : BULK INGREDIENT

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02

BioAsia
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BioAsia
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ETODOLAC

NDC Package Code : 17373-0187

Start Marketing Date : 2017-01-02

End Marketing Date : 2024-12-31

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

Marketing Category : BULK INGREDIENT

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BioAsia
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BioAsia
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06

BioAsia
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07

BioAsia
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BioAsia
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ETODOLAC

NDC Package Code : 11722-064

Start Marketing Date : 2017-01-18

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

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08

BioAsia
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BioAsia
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ETODOLAC

NDC Package Code : 81999-0013

Start Marketing Date : 2024-06-14

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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09

BioAsia
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ETODOLAC

NDC Package Code : 67628-1001

Start Marketing Date : 2013-08-09

End Marketing Date : 2025-12-31

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

Marketing Category : BULK INGREDIENT

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Looking for 41340-25-4 / Etodolac API manufacturers, exporters & distributors?

Etodolac manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Etodolac

Synonyms

41340-25-4, Etodolic acid, Lodine, Ultradol, Lodine xl, Ay-24236

Cas Number

41340-25-4

Unique Ingredient Identifier (UNII)

2M36281008

About Etodolac

A non-steroidal anti-inflammatory agent and cyclooxygenase-2 (COX-2) inhibitor with potent analgesic and anti-arthritic properties. It has been shown to be effective in the treatment of OSTEOARTHRITIS; RHEUMATOID ARTHRITIS; ANKYLOSING SPONDYLITIS; and in the alleviation of postoperative pain (PAIN, POSTOPERATIVE).

Etodolac Manufacturers

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

Etodolac Suppliers

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

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

Etodolac 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 Etodolac as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Etodolac Manufacturers | Traders | Suppliers

Etodolac Manufacturers, Traders, Suppliers 1
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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.