01 1Aurobindo Pharma Limited
02 1Glenmark Life Sciences Limited
03 1HETERO DRUGS LIMITED
04 1Unichem Laboratories Limited, India
01 1SOLRIAMFETOL HYDROCHLORIDE
02 3Solriamfetol Hydrochloride
01 4India
NDC Package Code : 59651-756
Start Marketing Date : 2023-11-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-953
Start Marketing Date : 2020-09-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0140
Start Marketing Date : 2019-12-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-100
Start Marketing Date : 2022-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Solriamfetol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Solriamfetol Hydrochloride, including repackagers and relabelers. The FDA regulates Solriamfetol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Solriamfetol Hydrochloride 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 Solriamfetol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Solriamfetol Hydrochloride supplier is an individual or a company that provides Solriamfetol Hydrochloride active pharmaceutical ingredient (API) or Solriamfetol Hydrochloride finished formulations upon request. The Solriamfetol Hydrochloride suppliers may include Solriamfetol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Solriamfetol Hydrochloride 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 Solriamfetol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Solriamfetol Hydrochloride 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 Solriamfetol Hydrochloride 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 Solriamfetol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Solriamfetol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Solriamfetol Hydrochloride suppliers with NDC on PharmaCompass.
We have 4 companies offering Solriamfetol Hydrochloride
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