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List of API Suppliers of MolPort-001-759-084 API listed on PharmaCompass.com

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Application Number
11405
R1-CEP 2013-134 - Rev 02
225MF10101
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ETODOLAC
Etodolac
Etodolac at 19 Pellinska Str. 83-20...
Issue/Submission Date
1995-03-29
2023-02-07
2013-05-10
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Jai Radhe Sales

Cophex 2024

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Octavius Pharma

Cophex 2024

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Application Number
5795
Status
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N/A
 
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ETODOLAC
Issue/Submission Date
1985-04-10
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Application Number
16789
CEP 2009-338 - Rev 02
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ETODOLAC
Etodolac, Micronised, non-micronise...
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2003-08-25
2023-09-27
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Application Number
15339
R1-CEP 2004-082 - Rev 06
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ETODOLAC USP MICRONIZED
Etodolac, Micronised
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2001-04-13
2023-04-03
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Application Number
25808
Indian CDSCO WC-0226
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2022-07-02
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ETODOLAC USP
Etodolac USP
Issue/Submission Date
2012-03-27
2019-10-07
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Application Number
31967
R1-CEP 2015-180 - Rev 00
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Expired
2022-08-12
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ETODOLAC USP
Etodolac
Etodolac USP
Issue/Submission Date
2017-11-11
2023-05-02
2019-08-13
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Application Number
24936
Status
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ETODOLAC
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2011-05-12
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Application Number
9529
Status
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ETODOLAC
Issue/Submission Date
1992-01-29
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Application Number
5346
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ETODOLAC (ETODOLIC ACID)
Issue/Submission Date
1984-05-03
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Application Number
5405
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7-ETHYLTRYPTOPHOL (INTERMEDIATE FOR...
Issue/Submission Date
1984-05-25
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Application Number
11359
Status
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N/A
 
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ETODOLAC
Issue/Submission Date
1995-02-20
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Application Number
21449
CEP 2008-175 - Rev 04
Indian CDSCO WC-0091
Status
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N/A
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Valid
2025-07-02
Filing Details
ETODOLAC
Etodolac
Etodolac (BP/USP/ Ph.Eur)
Issue/Submission Date
2008-04-16
2023-09-21
2022-06-08
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Application Number
24868
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ETODOLAC USP (ED6 PROCESS)
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2011-05-02
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Application Number
27512
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ETODOLAC USP (ED7 PROCESS)
Issue/Submission Date
2013-09-21
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Application Number
11740
Status
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N/A
 
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ETODOLAC
Issue/Submission Date
1995-11-06
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Application Number
24422
R1-CEP 2014-131 - Rev 00
Indian CDSCO WC-0180
Status
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Valid
 
Valid
2025-07-26
Filing Details
ETODOLAC USP
Etodolac
Etodolac (BP/USP/Ph. Eur.)
Issue/Submission Date
2010-12-07
2020-09-30
2022-08-29
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Application Number
5383
Status
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N/A
 
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ETODOLAC MICRONIZED AS PROCESSED IN...
Issue/Submission Date
1984-06-01
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Application Number
11766
R1-CEP 2000-331 - Rev 06
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ETODOLAC
Etodolac
Issue/Submission Date
1995-12-11
2014-04-29
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Application Number
21578
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ETODOLAC USP
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2008-04-28
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Application Number
23688
R1-CEP 2017-017 - Rev 00
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N/A
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ETODOLAC USP
Etodolac
Issue/Submission Date
2010-04-05
2023-01-19
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Application Number
5437
Status
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N/A
 
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ETODOLAC INTERMEDIATES
Issue/Submission Date
1984-06-22
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Application Number
14298
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ETODOLAC DRUG SUBSTANCE
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1999-07-16
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Application Number
12618
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ETODOLAC DRUG SUBSTANCE
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1997-08-08
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Application Number
R0-CEP 2013-084 - Rev 01
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Etodolac
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2015-02-13
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227MF10244
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Etodolac \"Teva / PLIVA2\" at Prila...
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Looking for 41340-25-4 / Etodolac API manufacturers, exporters & distributors?

Etodolac manufacturers, exporters & distributors 1

33

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).

MolPort-001-759-084 Manufacturers

A MolPort-001-759-084 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-759-084, including repackagers and relabelers. The FDA regulates MolPort-001-759-084 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-759-084 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 MolPort-001-759-084 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-759-084 Suppliers

A MolPort-001-759-084 supplier is an individual or a company that provides MolPort-001-759-084 active pharmaceutical ingredient (API) or MolPort-001-759-084 finished formulations upon request. The MolPort-001-759-084 suppliers may include MolPort-001-759-084 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-759-084 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

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.
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