Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
01 1Granules India Limited
02 1Benechim
03 1Moehs Catalana SL
04 1Assia Chemical Industries Ltd - Teva Tech Site
05 1Aurobindo Pharma Limited
06 1CTX Lifesciences Pvt. Ltd.
07 1Hetero Drugs Limited
08 1Indoco Remedies Limited
09 1Ipca Laboratories Limited
10 1MSN Life Sciences Private Limited
11 1SUN PHARMACEUTICAL INDUSTRIES, INC.
12 1YiChang HEC ChangJiang Pharmaceutical Co., Ltd.
13 2Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
14 1Zhejiang Hisoar Chuannan Pharmaceutical Co., Ltd.
15 1Zhejiang Huahai Pharmaceutical Co., Ltd.
01 2METOPROLOL
02 3METOPROLOL SUCCINATE
03 10Metoprolol Succinate
04 1metoprolol succinate
01 5China
02 8India
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
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 : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62756-659
Start Marketing Date : 2019-09-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
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
A Metoprolol Succinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metoprolol Succinate, including repackagers and relabelers. The FDA regulates Metoprolol Succinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metoprolol Succinate 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 Metoprolol Succinate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metoprolol Succinate supplier is an individual or a company that provides Metoprolol Succinate active pharmaceutical ingredient (API) or Metoprolol Succinate finished formulations upon request. The Metoprolol Succinate suppliers may include Metoprolol Succinate API manufacturers, exporters, distributors and traders.
click here to find a list of Metoprolol Succinate 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 Metoprolol Succinate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Metoprolol Succinate 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 Metoprolol Succinate 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 Metoprolol Succinate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Metoprolol Succinate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Metoprolol Succinate suppliers with NDC on PharmaCompass.
We have 14 companies offering Metoprolol Succinate
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