Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Limited
02 1Dr.Reddy's Laboratories Limited
03 1Benechim
04 1Moehs Catalana SL
05 1Assia Chemical Industries Ltd - Teva Tech Site
06 1Aurobindo Pharma Limited
07 1CTX Lifesciences Pvt. Ltd.
08 1Hetero Drugs Limited
09 1Indoco Remedies Limited
10 1Ipca Laboratories Limited
11 1MSN Life Sciences Private Limited
12 1SUN PHARMACEUTICAL INDUSTRIES, INC.
13 1YiChang HEC ChangJiang Pharmaceutical Co., Ltd.
14 2Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
15 1Zhejiang Hisoar Chuannan Pharmaceutical Co., Ltd.
16 1Zhejiang Huahai Pharmaceutical Co., Ltd.
17 1Zydus Lifesciences Limited
01 2METOPROLOL
02 3METOPROLOL SUCCINATE
03 11Metoprolol Succinate
04 1Metoprolol succinate
05 1metoprolol succinate
01 5China
02 10India
03 1Israel
04 2Spain
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
NDC Package Code : 62207-970
Start Marketing Date : 2021-03-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-851
Start Marketing Date : 2005-05-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0713
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 53335-0005
Start Marketing Date : 2017-03-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42419-003
Start Marketing Date : 2008-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49587-114
Start Marketing Date : 2019-12-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14445-022
Start Marketing Date : 2021-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1147
Start Marketing Date : 2012-05-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12666-0002
Start Marketing Date : 2008-02-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12666-0002
Start Marketing Date : 2006-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
80
PharmaCompass offers a list of Metoprolol Succinate 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 Metoprolol Succinate manufacturer or Metoprolol Succinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Metoprolol Succinate manufacturer or Metoprolol Succinate supplier.
PharmaCompass also assists you with knowing the Metoprolol Succinate API Price utilized in the formulation of products. Metoprolol Succinate API Price is not always fixed or binding as the Metoprolol Succinate Price is obtained through a variety of data sources. The Metoprolol Succinate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Seloken ZOC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Seloken ZOC, including repackagers and relabelers. The FDA regulates Seloken ZOC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Seloken ZOC 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 Seloken ZOC manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Seloken ZOC supplier is an individual or a company that provides Seloken ZOC active pharmaceutical ingredient (API) or Seloken ZOC finished formulations upon request. The Seloken ZOC suppliers may include Seloken ZOC API manufacturers, exporters, distributors and traders.
click here to find a list of Seloken ZOC suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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 Seloken ZOC as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Seloken ZOC API and other APIs are published in this directory by the FDA.
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 Seloken ZOC 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.
The NDC directory also contains data on finished compounded human drug products that contain Seloken ZOC and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Seloken ZOC NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Seloken ZOC suppliers with NDC on PharmaCompass.
We have 16 companies offering Seloken ZOC
Get in contact with the supplier of your choice:
