DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Reset all filters
01 1Dr.Reddy's Laboratories Limited
02 1Glenmark Life Sciences Limited
03 1Hetero Drugs Limited
04 1Indoco Remedies Limited
05 1Ipca Laboratories Limited
06 1MSN Life Sciences Private Limited
07 1Shandong Xinhua Pharmaceutical Co., Ltd.
08 2USV Private Limited
Reset all filters
01 9Glimepiride
Reset all filters
01 1China
02 8India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-041
Start Marketing Date : 2003-11-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-800
Start Marketing Date : 2004-08-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0010
Start Marketing Date : 1995-11-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14445-018
Start Marketing Date : 2009-01-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1151
Start Marketing Date : 2012-02-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72640-019
Start Marketing Date : 2021-03-30
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 58624-0708
Start Marketing Date : 2024-05-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62147-0300
Start Marketing Date : 2009-09-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62147-0009
Start Marketing Date : 2009-09-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
33
PharmaCompass offers a list of Glimepiride 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 Glimepiride manufacturer or Glimepiride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Glimepiride manufacturer or Glimepiride supplier.
PharmaCompass also assists you with knowing the Glimepiride API Price utilized in the formulation of products. Glimepiride API Price is not always fixed or binding as the Glimepiride Price is obtained through a variety of data sources. The Glimepiride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Glemax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Glemax, including repackagers and relabelers. The FDA regulates Glemax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Glemax 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 Glemax manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Glemax supplier is an individual or a company that provides Glemax active pharmaceutical ingredient (API) or Glemax finished formulations upon request. The Glemax suppliers may include Glemax API manufacturers, exporters, distributors and traders.
click here to find a list of Glemax 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 Glemax as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Glemax 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 Glemax 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 Glemax and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Glemax NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Glemax suppliers with NDC on PharmaCompass.
We have 8 companies offering Glemax
Get in contact with the supplier of your choice: