loader
Please Wait
Applying Filters...

Athena Athena

X

List of Drug Master Files (JDMF) for MolPort-001-888-120 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

Client Email Product
Menu
Filters Filter
Cross PopUp
FILTER :

filter

01 Arch Pharmalabs Limited (1)

02 Watson Pharma Private Limited (1)

filter

01 Piroxicam (2)

filter

01 India (1)

02 Ireland (1)

URL Supplier Web Content
220MF10258
201/301, Corporate Enclave, HDO-Cor...
2008-12-22
2008-12-22
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content
URL Supplier Web Content
221MF10166
505 Hyde Park, Chandivali Junction,...
2009-07-30
2009-07-30
ASK
US
PHARMACOMPASS
Upload
your Marketing & Sales content

Looking for 36322-90-4 / Piroxicam API manufacturers, exporters & distributors?

Piroxicam manufacturers, exporters & distributors 1

72

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

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

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

API | Excipient name

Piroxicam

Synonyms

36322-90-4, Feldene, Piroxicamum, Pyroxycam, Roxicam, Piroftal

Cas Number

36322-90-4

Unique Ingredient Identifier (UNII)

13T4O6VMAM

About Piroxicam

A cyclooxygenase inhibiting, non-steroidal anti-inflammatory agent (NSAID) that is well established in treating rheumatoid arthritis and osteoarthritis and used for musculoskeletal disorders, dysmenorrhea, and postoperative pain. Its long half-life enables it to be administered once daily.

MolPort-001-888-120 Manufacturers

A MolPort-001-888-120 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-888-120, including repackagers and relabelers. The FDA regulates MolPort-001-888-120 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-888-120 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-001-888-120 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-888-120 Suppliers

A MolPort-001-888-120 supplier is an individual or a company that provides MolPort-001-888-120 active pharmaceutical ingredient (API) or MolPort-001-888-120 finished formulations upon request. The MolPort-001-888-120 suppliers may include MolPort-001-888-120 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-888-120 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-888-120 JDMF

The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

The MolPort-001-888-120 Drug Master File in Japan (MolPort-001-888-120 JDMF) empowers MolPort-001-888-120 API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

PMDA reviews the MolPort-001-888-120 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-888-120 JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

click here to find a list of MolPort-001-888-120 suppliers with JDMF on PharmaCompass.

MolPort-001-888-120 Manufacturers | Traders | Suppliers

MolPort-001-888-120 Manufacturers, Traders, Suppliers 1
11

We have 2 companies offering MolPort-001-888-120

Get in contact with the supplier of your choice:

  1. Actavis Inc
  2. Arch Pharmalabs
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.
Post Enquiry
POST ENQUIRY