01 1Glenmark Life Sciences Limited
02 1MYLAN LABORATORIES LIMITED
03 1Sionc Pharmaceutical Private Limited
04 1Viyash Life Sciences Private Limited
01 1FROVATRIPTAN SUCCINATE
02 1FROVATRIPTAN SUCCINATE MONOHYDRATE
03 2Frovatriptan Succinate
01 3India
02 1U.S.A
NDC Package Code : 66039-865
Start Marketing Date : 2009-07-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 76055-0008
Start Marketing Date : 2019-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-780
Start Marketing Date : 2015-02-19
End Marketing Date : 2026-12-01
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82245-0110
Start Marketing Date : 2001-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Frovatriptan Succinate Hydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Frovatriptan Succinate Hydrate, including repackagers and relabelers. The FDA regulates Frovatriptan Succinate Hydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Frovatriptan Succinate Hydrate supplier is an individual or a company that provides Frovatriptan Succinate Hydrate active pharmaceutical ingredient (API) or Frovatriptan Succinate Hydrate finished formulations upon request. The Frovatriptan Succinate Hydrate suppliers may include Frovatriptan Succinate Hydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate 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 Frovatriptan Succinate Hydrate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Frovatriptan Succinate Hydrate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Frovatriptan Succinate Hydrate suppliers with NDC on PharmaCompass.
We have 4 companies offering Frovatriptan Succinate Hydrate
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
