Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 1,320Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1Dr. Reddy's Laboratories Limited

02 1Neuland Laboratories Limited

03 1Teva API India Private Ltd

04 2Aurobindo Pharma Limited

05 1Dasami Lab Private Limited

06 3Glenmark Life Sciences Limited

07 1HETERO LABS LIMITED

08 1Hetero Labs Limited

09 1MSD International GmbH (Singapore Branch)

10 1MSN Laboratories Private Limited

11 1MYLAN LABORATORIES LIMITED

12 2Nantong Chanyoo Pharmatech Co., Ltd

13 1Symed Labs Limited

14 1Synthimed Labs Private Limited

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

EZETIMIBE

NDC Package Code : 55111-079

Start Marketing Date : 2014-11-05

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (2kg/2kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothNeuland Laboratories- A dedicated 100% API provider.

EZETIMIBE

NDC Package Code : 58032-2004

Start Marketing Date : 2017-12-14

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Neuland

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

EZETIMIBE

NDC Package Code : 15894-0011

Start Marketing Date : 2017-11-17

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

TAPI Company Banner

04

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
Not Confirmed

EZETIMIBE

NDC Package Code : 59651-056

Start Marketing Date : 2024-01-12

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (50kg/50kg)

Marketing Category : BULK INGREDIENT

blank

05

The Generic Rx Session
Not Confirmed
arrow
arrow
The Generic Rx Session
Not Confirmed

EZETIMIBE

NDC Package Code : 59651-698

Start Marketing Date : 2024-01-11

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (50kg/50kg)

Marketing Category : BULK INGREDIENT

blank

06

PharmScience R&D
Not Confirmed
arrow
arrow
PharmScience R&D
Not Confirmed

EZETIMIBE

NDC Package Code : 66039-839

Start Marketing Date : 2006-08-30

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

blank

07

The Generic Rx Session
Not Confirmed
arrow

08

PharmScience R&D
Not Confirmed
arrow
arrow
PharmScience R&D
Not Confirmed

EZETIMIBE

NDC Package Code : 66022-0212

Start Marketing Date : 2023-12-13

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

blank

09

PharmScience R&D
Not Confirmed
arrow

10

PharmScience R&D
Not Confirmed
arrow
arrow
PharmScience R&D
Not Confirmed

EZETIMIBE

NDC Package Code : 65015-812

Start Marketing Date : 2015-01-13

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

blank

Looking for 163222-33-1 / Ezetimibe API manufacturers, exporters & distributors?

Ezetimibe manufacturers, exporters & distributors 1

15

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

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

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

API | Excipient name

Ezetimibe

Synonyms

163222-33-1, Zetia, Ezetrol, Ezedoc, Sch 58235, Sch58235

Cas Number

163222-33-1

Unique Ingredient Identifier (UNII)

EOR26LQQ24

About Ezetimibe

An azetidine derivative and ANTICHOLESTEREMIC AGENT that inhibits intestinal STEROL absorption. It is used to reduce total CHOLESTEROL; LDL CHOLESTEROL, and APOLIPOPROTEINS B in the treatment of HYPERLIPIDEMIAS.

VYTORIN Manufacturers

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

VYTORIN Suppliers

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

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

VYTORIN 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 VYTORIN as an active pharmaceutical ingredient (API).

Finished drug products

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

click here to find a list of VYTORIN suppliers with NDC on PharmaCompass.

VYTORIN Manufacturers | Traders | Suppliers

VYTORIN Manufacturers, Traders, Suppliers 1
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.