Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
01 1Evonik Corporation
02 1Dr.Reddy's Laboratories Limited
03 1Moehs BCN SL
04 1SCI PHARMTECH, INC.
05 2Aurobindo Pharma Limited
06 1Hetero Drugs Limited
07 1Jubilant Pharmova Limited
08 1MSN Laboratories Private Limited
09 1MYLAN LABORATORIES LIMITED
10 2Olon SpA
11 1Professional Compounding Centers of America dba PCCA
12 1R.L.Fine Chem Private Limited
13 1SHODHANA LABORATPORIES PRIVATE LIMITED
14 1Uquifa Spain
15 1YiChang HEC ChangJiang Pharmaceutical Co.,Ltd.
01 3DULOXETINE HYDROCHLORIDE
02 1Duloxetine
03 2Duloxetine HCl
04 8Duloxetine Hydrochloride
05 1Duloxetine Hydrochloride (Process II)
06 1Duloxetine hydrochloride
07 1duloxetin hydrochloride
01 1China
02 1Germany
03 8India
04 2Italy
05 2Spain
06 1Taiwan
07 1U.S.A
08 1United Kingdom
Evonik's CDMO solutions for APIs and HPAPIs: It specializes where the client needs it most!
NDC Package Code : 62128-0386
Start Marketing Date : 2004-08-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-859
Start Marketing Date : 2007-02-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 71495-0003
Start Marketing Date : 2022-02-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
NDC Package Code : 68108-0705
Start Marketing Date : 2012-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49587-111
Start Marketing Date : 2016-06-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14501-0005
Start Marketing Date : 2010-03-24
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0017
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0046
Start Marketing Date : 2012-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0059
Start Marketing Date : 2021-03-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49711-1507
Start Marketing Date : 2009-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Duloxetine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Duloxetine Hydrochloride, including repackagers and relabelers. The FDA regulates Duloxetine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Duloxetine 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 Duloxetine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Duloxetine Hydrochloride supplier is an individual or a company that provides Duloxetine Hydrochloride active pharmaceutical ingredient (API) or Duloxetine Hydrochloride finished formulations upon request. The Duloxetine Hydrochloride suppliers may include Duloxetine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Duloxetine 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 Duloxetine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Duloxetine 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 Duloxetine 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 Duloxetine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Duloxetine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Duloxetine Hydrochloride suppliers with NDC on PharmaCompass.
We have 15 companies offering Duloxetine Hydrochloride
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