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Looking for 5967-84-0 / Theophylline Monohydrate API manufacturers, exporters & distributors?

Theophylline Monohydrate manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Theophylline Monohydrate

Synonyms

5967-84-0, Quibron, Theolair-sr, Theochron, 1,3-dimethylxanthine monohydrate, Theophylline (monohydrate)

Cas Number

5967-84-0

Unique Ingredient Identifier (UNII)

C137DTR5RG

About Theophylline Monohydrate

A methyl xanthine derivative from tea with diuretic, smooth muscle relaxant, bronchial dilation, cardiac and central nervous system stimulant activities. Theophylline inhibits the 3',5'-CYCLIC NUCLEOTIDE PHOSPHODIESTERASE that degrades CYCLIC AMP thus potentiates the actions of agents that act through ADENYLYL CYCLASES and cyclic AMP.

Theophylline Monohydrate Manufacturers

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

Theophylline Monohydrate Suppliers

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

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

Theophylline Monohydrate GMP

Theophylline Monohydrate Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

PharmaCompass offers a list of Theophylline Monohydrate GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Theophylline Monohydrate GMP manufacturer or Theophylline Monohydrate GMP API supplier for your needs.

Theophylline Monohydrate CoA

A Theophylline Monohydrate CoA (Certificate of Analysis) is a formal document that attests to Theophylline Monohydrate's compliance with Theophylline Monohydrate specifications and serves as a tool for batch-level quality control.

Theophylline Monohydrate CoA mostly includes findings from lab analyses of a specific batch. For each Theophylline Monohydrate CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

Theophylline Monohydrate may be tested according to a variety of international standards, such as European Pharmacopoeia (Theophylline Monohydrate EP), Theophylline Monohydrate JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Theophylline Monohydrate USP).

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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