LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 1LGM Pharma
02 1DKSH
03 1HRV Global Life Sciences
04 1Nortec Quimica
05 1Arene Lifesciences
06 1Aurobindo Pharma Limited
07 1Aurore Life Sciences
08 1Blanver
09 1Cambrex Corporation
10 1Chromo Laboratories
11 2Cipla
12 1Dasami Lab
13 1Emcure Pharmaceuticals
14 1Gilead Sciences
15 1Guangzhou Tosun Pharmaceutical
16 1HONOUR LAB LTD
17 3Hetero Drugs
18 1Laurus Labs
19 1Lupin Ltd
20 1Macleods Pharmaceuticals Limited
21 1Mangalam Drugs & Organics Ltd
22 1RANBAXY LABORATORIES LIMITED
23 1Shanghai Desano Bio-Pharmaceutical
24 1Shijiazhuang Lonzeal Pharmac.Co. ltd
25 3Viatris
26 1Vivin Drugs
01 2Brazil
02 3China
03 19India
04 1Switzerland
05 6U.S.A
01 13Active
02 4Inactive
03 14Blank
01 31Blank
01 1229MF10061
02 1229MF10167
03 29Blank
01 1WC-0016
02 1WC-0023
03 1WC-0041
04 1WC-0065
05 1WC-0065a
06 1WC-0079
07 2WC-0117
08 1WC-0119
09 1WC-0140
10 1WC-0141
11 1WC-0201
12 1WC-0213
13 1WC-0473
14 1WC-0578
15 16Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34105
Submission : 2019-10-17
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-11-05
Pay. Date : 2013-02-07
DMF Number : 25617
Submission : 2011-12-19
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32096
Submission : 2017-11-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24975
Submission : 2011-05-18
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28505
Submission : 2014-08-04
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21706
Submission : 2008-06-17
Status : Inactive
Type : II
A Emtricitabine / Tenofovir manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Emtricitabine / Tenofovir, including repackagers and relabelers. The FDA regulates Emtricitabine / Tenofovir manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Emtricitabine / Tenofovir 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 Emtricitabine / Tenofovir supplier is an individual or a company that provides Emtricitabine / Tenofovir active pharmaceutical ingredient (API) or Emtricitabine / Tenofovir finished formulations upon request. The Emtricitabine / Tenofovir suppliers may include Emtricitabine / Tenofovir API manufacturers, exporters, distributors and traders.
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