Inke S.A: APIs manufacturing plant.
01 1INKE SA
02 1Aurobindo Pharma Limited
03 1Emcure Pharmaceuticals Limited
04 1Glenmark Life Sciences Limited
05 1Hetero Drugs Limited
06 1Jubilant Pharmova Limited
07 1MYLAN LABORATORIES LIMITED
08 1Natco Pharma Limited
09 1Pliva Croatia Ltd
10 1SMS Pharmaceuticals Limited
11 1Tianish Laboratories Private Limited
01 3ZOLMITRIPTAN
02 7Zolmitriptan
03 1zolmitriptan
01 1Croatia
02 8India
03 1Spain
04 1U.S.A
Inke S.A: APIs manufacturing plant.
NDC Package Code : 64567-0016
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-845
Start Marketing Date : 2008-12-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-801
Start Marketing Date : 2024-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-863
Start Marketing Date : 2023-12-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0050
Start Marketing Date : 1997-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1145
Start Marketing Date : 2010-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63850-4322
Start Marketing Date : 2016-01-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 11722-012
Start Marketing Date : 2017-12-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67835-5007
Start Marketing Date : 2008-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-688
Start Marketing Date : 2015-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Zolmitriptan API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Zolmitriptan manufacturer or Zolmitriptan supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Zolmitriptan manufacturer or Zolmitriptan supplier.
PharmaCompass also assists you with knowing the Zolmitriptan API Price utilized in the formulation of products. Zolmitriptan API Price is not always fixed or binding as the Zolmitriptan Price is obtained through a variety of data sources. The Zolmitriptan Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Zomigoro manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zomigoro, including repackagers and relabelers. The FDA regulates Zomigoro manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zomigoro 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 Zomigoro manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zomigoro supplier is an individual or a company that provides Zomigoro active pharmaceutical ingredient (API) or Zomigoro finished formulations upon request. The Zomigoro suppliers may include Zomigoro API manufacturers, exporters, distributors and traders.
click here to find a list of Zomigoro 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 Zomigoro as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Zomigoro 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 Zomigoro 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 Zomigoro and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Zomigoro NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Zomigoro suppliers with NDC on PharmaCompass.
We have 11 companies offering Zomigoro
Get in contact with the supplier of your choice:
