01 1DARMERICA, LLC
02 1Hefei Lifeon Pharmaceutical Co., Ltd. (API branch)
03 1Medisca Inc.
04 1Piramal Pharma Limited
05 1Professional Compounding Centers of America dba PCCA
01 12,3-Dimercaptosuccinic Acid (DMSA)
02 1DIMERCAPTOSUCCINIC ACID
03 3Succimer
01 1China
02 3U.S.A
03 1United Kingdom
NDC Package Code : 71052-011
Start Marketing Date : 2020-06-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1000g/1000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70086-124
Start Marketing Date : 2019-07-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0780
Start Marketing Date : 2014-07-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0108
Start Marketing Date : 2019-12-26
End Marketing Date : 2025-01-04
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 65085-0072
Start Marketing Date : 2020-11-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Succimer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Succimer, including repackagers and relabelers. The FDA regulates Succimer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Succimer API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Succimer supplier is an individual or a company that provides Succimer active pharmaceutical ingredient (API) or Succimer finished formulations upon request. The Succimer suppliers may include Succimer API manufacturers, exporters, distributors and traders.
click here to find a list of Succimer 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 Succimer as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Succimer 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 Succimer 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 Succimer and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Succimer NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Succimer suppliers with NDC on PharmaCompass.
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