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CILASTATIN; IMIPENEM ANHYDROUS; RELEBACTAM ANHYDROUS

NDC Package Code : 0006-0138

Start Marketing Date : 2020-01-06

End Marketing Date : 2025-12-31

Dosage Form (Strength) : INJECTION, POWDER, FOR SOLUTION (500mg/100mL 500mg/100mL 250mg/100mL)

Marketing Category : DRUG FOR FURTHER PROCESSING

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Looking for 82009-34-5 / Cilastatin API manufacturers, exporters & distributors?

Cilastatin manufacturers, exporters & distributors 1

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

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

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

API | Excipient name

Cilastatin

Synonyms

82009-34-5, Cilastatina, Cilastatine, Cilastatinum, Mk-791, Cilastatin (inn)

Cas Number

82009-34-5

Unique Ingredient Identifier (UNII)

141A6AMN38

About Cilastatin

A renal dehydropeptidase-I and leukotriene D4 dipeptidase inhibitor. Since the antibiotic, IMIPENEM, is hydrolyzed by dehydropeptidase-I, which resides in the brush border of the renal tubule, cilastatin is administered with imipenem to increase its effectiveness. The drug also inhibits the metabolism of leukotriene D4 to leukotriene E4.

0791, MK Manufacturers

A 0791, MK manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 0791, MK, including repackagers and relabelers. The FDA regulates 0791, MK manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 0791, MK 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 0791, MK manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

0791, MK Suppliers

A 0791, MK supplier is an individual or a company that provides 0791, MK active pharmaceutical ingredient (API) or 0791, MK finished formulations upon request. The 0791, MK suppliers may include 0791, MK API manufacturers, exporters, distributors and traders.

click here to find a list of 0791, MK suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

0791, MK 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 0791, MK as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for 0791, MK 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 0791, MK 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 0791, MK and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a 0791, MK NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of 0791, MK suppliers with NDC on PharmaCompass.

0791, MK Manufacturers | Traders | Suppliers

0791, MK Manufacturers, Traders, Suppliers 1
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We have 1 companies offering 0791, MK

Get in contact with the supplier of your choice:

  1. Merck & Co
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.