DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
02 1Alivus Life Sciences Limited
03 1Amoli Organics (A Division of Umedica Laboratories Pvt.Ltd.)
04 1Astellas Ireland Co., Limited
05 1Aurobindo Pharma Limited
06 1Cipla Ltd.
07 1Hetero Drugs Limited
08 1Jubilant Biosys limited
09 1MSN Laboratories Private Limited
10 1Optimus Drugs Private Limited
11 1SMS Pharmaceuticals Limited
12 1Unichem Laboratories Limited, India
01 2SOLIFENACIN SUCCINATE
02 1Solifenacin
03 5Solifenacin Succinate
04 1Solifenacin Succinate API
05 1Solifenacin succinate
06 2solifenacin succinate
01 11India
02 1Japan
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-895
Start Marketing Date : 2008-12-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62512-0054
Start Marketing Date : 2017-09-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57438-8096
Start Marketing Date : 2005-01-05
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65862-800
Start Marketing Date : 2024-01-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7705
Start Marketing Date : 2016-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0042
Start Marketing Date : 2004-11-19
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65372-1158
Start Marketing Date : 2011-03-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0053
Start Marketing Date : 2010-03-30
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-006
Start Marketing Date : 2015-04-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53747-067
Start Marketing Date : 2020-03-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Solifenacin Succinate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Solifenacin Succinate manufacturer or Solifenacin Succinate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Solifenacin Succinate manufacturer or Solifenacin Succinate supplier.
A vesicare manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of vesicare, including repackagers and relabelers. The FDA regulates vesicare manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. vesicare 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 vesicare manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A vesicare supplier is an individual or a company that provides vesicare active pharmaceutical ingredient (API) or vesicare finished formulations upon request. The vesicare suppliers may include vesicare API manufacturers, exporters, distributors and traders.
click here to find a list of vesicare suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 vesicare as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for vesicare 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 vesicare 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 vesicare and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a vesicare NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of vesicare suppliers with NDC on PharmaCompass.
We have 12 companies offering vesicare
Get in contact with the supplier of your choice:
