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List of Drug Master Files (JDMF) for MolPort-001-759-087 Active Pharmaceutical Ingredient (API) submitted to the Review Authority in Japan (PMDA). Original Data : PMDA Database

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01 COSMA S. P. A. (1)

02 Ipca Laboratories Limited (1)

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01 Propranolol hydrochloride (1)

02 Propranolol hydrochloride (production only) (1)

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01 India (1)

02 Italy (1)

URL Supplier Web Content
221MF10278
Via Colleoni 15/17, 24040 Ciserano ...
2016-03-11
2009-12-18
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218MF10174
48, Kandivli Industrial Estate, Kan...
2006-10-20
2006-02-08
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Looking for 318-98-9 / Propranolol Hydrochloride API manufacturers, exporters & distributors?

Propranolol Hydrochloride manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Propranolol Hydrochloride

Synonyms

318-98-9, Propranolol hcl, Inderal, Avlocardyl, Dociton, Inderalici

Cas Number

318-98-9

Unique Ingredient Identifier (UNII)

F8A3652H1V

About Propranolol Hydrochloride

A widely used non-cardioselective beta-adrenergic antagonist. Propranolol has been used for MYOCARDIAL INFARCTION; ARRHYTHMIA; ANGINA PECTORIS; HYPERTENSION; HYPERTHYROIDISM; MIGRAINE; PHEOCHROMOCYTOMA; and ANXIETY but adverse effects instigate replacement by newer drugs.

MolPort-001-759-087 Manufacturers

A MolPort-001-759-087 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MolPort-001-759-087, including repackagers and relabelers. The FDA regulates MolPort-001-759-087 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MolPort-001-759-087 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-001-759-087 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

MolPort-001-759-087 Suppliers

A MolPort-001-759-087 supplier is an individual or a company that provides MolPort-001-759-087 active pharmaceutical ingredient (API) or MolPort-001-759-087 finished formulations upon request. The MolPort-001-759-087 suppliers may include MolPort-001-759-087 API manufacturers, exporters, distributors and traders.

click here to find a list of MolPort-001-759-087 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

MolPort-001-759-087 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-001-759-087 Drug Master File in Japan (MolPort-001-759-087 JDMF) empowers MolPort-001-759-087 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-001-759-087 JDMF during the approval evaluation for pharmaceutical products. At the time of MolPort-001-759-087 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-001-759-087 suppliers with JDMF on PharmaCompass.

MolPort-001-759-087 Manufacturers | Traders | Suppliers

MolPort-001-759-087 Manufacturers, Traders, Suppliers 1
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We have 2 companies offering MolPort-001-759-087

Get in contact with the supplier of your choice:

  1. COSMA S.p.A
  2. Ipca Laboratories
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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