With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Teva API India Limited
03 1Alembic Pharmaceuticals Limited
04 1Assia Chemical Industries Ltd - Teva Tech Site
05 2Aurobindo Pharma Limited
06 1Cadila Pharmaceuticals Limited
07 1Erregierre SpA
08 1KALCHEM INTERNATIONAL INC
09 1LETCO MEDICAL, LLC
10 1Medisca Inc.
11 1Olon S.p.A.
12 1Olon SpA
13 1Professional Compounding Centers of America dba PCCA
14 1Quimica Sintetica S.A.
15 1Siegfried AG
16 1Spectrum Laboratory Products, Inc.
17 1Uquifa Spain
18 1Willow Birch Pharma, Inc
19 1Xenex Laboratories Inc
01 1FLUOXETINE HCL
02 3FLUOXETINE HYDROCHLORIDE
03 1FLUOXETINE hcl
04 1Fluoxetine
05 1Fluoxetine HCl
06 10Fluoxetine Hydrochloride
07 1Fluoxetine Hydrochloride Process II
08 1Fluoxetine Hydrochloride micronized
09 1fluoxetine hydrochloride
01 1Canada
02 1Finland
03 4India
04 2Israel
05 3Italy
06 2Spain
07 1Switzerland
08 5U.S.A
09 1United Kingdom
With Fermion, start the journey of your innovative API.
NDC Package Code : 12780-2945
Start Marketing Date : 1995-01-26
End Marketing Date : 2026-03-02
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
TAPI offers customized CDMO Solutions for API development and manufacturing services.
NDC Package Code : 15894-0039
Start Marketing Date : 2024-04-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46708-855
Start Marketing Date : 2012-03-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49706-0785
Start Marketing Date : 2010-01-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0013
Start Marketing Date : 2014-07-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0020
Start Marketing Date : 2012-12-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0517
Start Marketing Date : 2020-02-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17205-612
Start Marketing Date : 2008-07-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3176
Start Marketing Date : 2001-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 10695-173
Start Marketing Date : 2024-05-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Fluoxetine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluoxetine Hydrochloride, including repackagers and relabelers. The FDA regulates Fluoxetine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluoxetine 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 Fluoxetine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluoxetine Hydrochloride supplier is an individual or a company that provides Fluoxetine Hydrochloride active pharmaceutical ingredient (API) or Fluoxetine Hydrochloride finished formulations upon request. The Fluoxetine Hydrochloride suppliers may include Fluoxetine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Fluoxetine 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 Fluoxetine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Fluoxetine 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 Fluoxetine 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 Fluoxetine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Fluoxetine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Fluoxetine Hydrochloride suppliers with NDC on PharmaCompass.
We have 18 companies offering Fluoxetine Hydrochloride
Get in contact with the supplier of your choice:
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