LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 3Symbiotec Pharmalab
03 13M Drug Delivery Systems
04 1ASG Biochem
05 1Androst Biotech
06 1Arudavis Labs
07 1Balaji Corporation
08 4Bayer AG
09 1CHEMO
10 1Cipla
11 1Cohesion Biotec
12 1Curia
13 1FORTEQ NIDAU AG
14 1Formosa Laboratories
15 3Gedeon Richter
16 1Guangzhou Tosun Pharmaceutical
17 1Hangzhou Longshine Bio-Tech
18 1Hetero Drugs
19 1Hubei Gedian Humanwell Pharmaceutical
20 2Hunan KYX Pharmaceutical
21 1Indo Phyto Chemicals Private Ltd
22 3Industriale Chimica
23 1Jenapharm GmbH & Co KG DE 07745 Jena
24 1Jiangsu Lianhuan Pharmaceutical
25 2Lupin Ltd
26 1Naari
27 3Qinhuangdao Zizhu Pharmaceutical
28 2ScinoPharm Taiwan Ltd
29 2Sterling Chemical Malta
30 2Sterling Spa
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32 1Yangzhou Pharmaceutical Factory
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01 11China
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09 3Taiwan
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01 20Active
02 10Inactive
03 28Blank
01 9Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
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01 1221MF10183
02 1221MF10292
03 1228MF10159
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01 1HB230032
02 1WC-0161A2
03 1WC-0162Amended
04 1WC-0162n
05 2WC-0419
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01 112866-1010
02 112866-1011
03 122552-0047
04 144132-004
05 144132-012
06 145541-1149
07 145541-1174
08 151508-012
09 151508-203
10 153104-7669
11 159057-001
12 159057-002
13 160722-3025
14 163190-0130
15 163190-0660
16 163190-0850
17 164918-1907
18 164918-1940
19 165089-0036
20 165129-2003
21 166499-0018
22 181955-0027
23 36Blank
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-06-23
Pay. Date : 2014-01-23
DMF Number : 27867
Submission : 2014-01-27
Status : Active
Type : II
Date of Issue : 2022-06-30
Valid Till : 2025-07-02
Written Confirmation Number : WC-0161A2
Address of the Firm :
NDC Package Code : 22552-0047
Start Marketing Date : 2017-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
Date of Issue : 2022-07-23
Valid Till : 2025-02-07
Written Confirmation Number : WC-0162n
Address of the Firm :
Date of Issue : 2022-08-31
Valid Till : 2025-07-02
Written Confirmation Number : WC-0162Amended
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26830
Submission : 2013-01-31
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-12-02
Pay. Date : 2022-08-15
DMF Number : 33000
Submission : 2022-06-24
Status : Active
Type : II
Certificate Number : R0-CEP 2022-199 - Rev 00
Issue Date : 2023-05-19
Type : Chemical
Substance Number : 926
Status : Valid
Date of Issue : 2023-11-13
Valid Till : 2026-11-12
Written Confirmation Number : HB230032
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8806
Submission : 1990-10-30
Status : Active
Type : II
Certificate Number : R1-CEP 1999-141 - Rev 04
Issue Date : 2021-12-20
Type : Chemical
Substance Number : 926
Status : Valid
NDC Package Code : 45541-1149
Start Marketing Date : 2001-07-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9136
Submission : 1991-05-20
Status : Active
Type : II
NDC Package Code : 45541-1174
Start Marketing Date : 1995-04-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35419
Submission : 2020-12-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12934
Submission : 1998-03-20
Status : Inactive
Type : II
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PharmaCompass offers a list of Levonorgestrel API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Levonorgestrel manufacturer or Levonorgestrel supplier for your needs.
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A Triagynon manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triagynon, including repackagers and relabelers. The FDA regulates Triagynon manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triagynon 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 Triagynon supplier is an individual or a company that provides Triagynon active pharmaceutical ingredient (API) or Triagynon finished formulations upon request. The Triagynon suppliers may include Triagynon API manufacturers, exporters, distributors and traders.
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