LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 1LGM Pharma
02 1Fermion Oy
03 1Metrochem API Private Limited
04 1Temad Co
05 1Jai Radhe Sales
06 1HRV Global Life Sciences
07 1Zeon Pharma Industries India Pvt Ltd
08 1TAPI Technology & API Services
09 1Alembic Pharmaceuticals Limited
10 1Atomgrid
11 2Aurobindo Pharma Limited
12 1BASF Corp
13 1CHEMO
14 1Cadila Pharmaceuticals
15 1Changzhou Siyao Pharmaceuticals
16 1Cilag AG
17 2Eli Lilly
18 1Erregierre SpA
19 1Esteve Quimica
20 1Freemen Nutra
21 1Gedeon Richter
22 1Gurvey & Berry
23 1HELM Portugal
24 1Hengdian Group
25 1Industriale Chimica
26 1Natco Pharma
27 2Olon S.p.A
28 1Osmopharm
29 1Qingdao Qingmei Biotech
30 1Qualitek pharma
31 1Quimica Sintetica
32 1RA CHEM PHARMA LIMITED
33 1RANBAXY LABORATORIES LIMITED
34 1Recordati
35 1SIMS Srl
36 1Senores Pharmaceuticals
37 2Siegfried AG
38 1Sifavitor srl
39 1Smilax Laboratories Limited
40 1Synergene Active Ingredients Pvt Ltd
41 1Teva Pharmaceutical Industries
42 2UQUIFA
43 2Wockhardt
44 1Zim Laboratories
45 1elm-plastic GmbH
01 1Canada
02 4China
03 1Finland
04 1Germany
05 1Hungary
06 19India
07 1Iran
08 2Israel
09 7Italy
10 1Portugal
11 5Spain
12 4Switzerland
13 3U.S.A
14 1Blank
01 12Active
02 14Inactive
03 25Blank
01 11Valid
02 5Withdrawn by Holder
03 35Blank
01 51Blank
01 1WC-0017
02 1WC-0074
03 1WC-0081
04 48Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-10-13
Pay. Date : 2014-10-02
DMF Number : 11315
Submission : 1995-01-26
Status : Active
Type : II
Certificate Number : R1-CEP 2009-354 - Rev 02
Issue Date : 2020-12-21
Type : Chemical
Substance Number : 1104
Status : Valid
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
Registrant Name : Pharma Science Korea Co., Ltd.
Registration Date : 2014-10-14
Registration Number : 20141014-51-C-327-10
Manufacturer Name : Fermion Oy
Manufacturer Address : Orioninkatu 2, 10900 Hanko, Finland_x000D_
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-02-22
Pay. Date : 2017-02-06
DMF Number : 12146
Submission : 1996-10-02
Status : Active
Type : II
Certificate Number : R1-CEP 1997-042 - Rev 11
Issue Date : 2023-06-22
Type : Chemical
Substance Number : 1104
Status : Valid
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
Available Reg Filing : ASMF |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12631
Submission : 1997-08-27
Status : Inactive
Type : II
NDC Package Code : 49711-1502
Start Marketing Date : 2009-10-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Bansen Co., Ltd.
Registration Date : 2018-06-25
Registration Number : 20050831-51-C-175-04(15)
Manufacturer Name : Union Quimico Farmaceutica, SA
Manufacturer Address : Poli Industrial El Pla Av. Puigcerda, 9 C-17, km 17.4 08185 Llica de Vall (Barcelona) Spain
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15770
Submission : 2001-12-14
Status : Inactive
Type : II
NDC Package Code : 49711-1502
Start Marketing Date : 2009-10-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Bansen Co., Ltd.
Registration Date : 2018-06-25
Registration Number : 20050831-51-C-175-04(15)
Manufacturer Name : Union Quimico Farmaceutica, SA
Manufacturer Address : Poli Industrial El Pla Av. Puigcerda, 9 C-17, km 17.4 08185 Llica de Vall (Barcelona) Spain
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.
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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.
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