Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 2Moehs Catalana SL
02 1Moehs Catalana, S.L.
03 1Assia Chemical Industries Ltd - Teva Tech Site
04 1Aurobindo Pharma Limited
05 1CTX Lifesciences Pvt. Ltd.
06 1Fagron Inc
07 1Ipca Laboratories Limited
08 1MSN Life Sciences Private Limited
09 1Medisca Inc.
10 1Professional Compounding Centers of America dba PCCA
11 1Societa Italiana Medicinali Scandicci S.I.M.S., SrL
12 1Spectrum Laboratory Products, Inc.
13 1Zhejiang Apeloa Jiayuan Pharmaceutical Co., Ltd.
01 1Lidocaine
02 3METOPROLOL TARTRATE
03 1METOPROLOL TARTRATE DS/IP
04 8Metoprolol Tartrate
05 1metoprolol tartrate
01 1China
02 4India
03 1Israel
04 1Italy
05 1Netherlands
06 3Spain
07 2U.S.A
08 1United Kingdom
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0710
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 : 52932-0743
Start Marketing Date : 2013-06-27
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 : 52932-0721
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42419-009
Start Marketing Date : 2009-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0915
Start Marketing Date : 2004-09-01
End Marketing Date : 2025-05-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 38779-0578
Start Marketing Date : 2017-08-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-2697
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12660-0005
Start Marketing Date : 1979-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-4718
Start Marketing Date : 1996-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12666-0009
Start Marketing Date : 2009-12-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Metoprolol Tartrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metoprolol Tartrate, including repackagers and relabelers. The FDA regulates Metoprolol Tartrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metoprolol Tartrate 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 Tartrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metoprolol Tartrate supplier is an individual or a company that provides Metoprolol Tartrate active pharmaceutical ingredient (API) or Metoprolol Tartrate finished formulations upon request. The Metoprolol Tartrate suppliers may include Metoprolol Tartrate API manufacturers, exporters, distributors and traders.
click here to find a list of Metoprolol Tartrate 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 Tartrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Metoprolol Tartrate 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 Tartrate 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 Tartrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Metoprolol Tartrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Metoprolol Tartrate suppliers with NDC on PharmaCompass.
We have 12 companies offering Metoprolol Tartrate
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