LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 1Jai Radhe Sales
03 1Virupaksha Organics
04 1HRV Global Life Sciences
05 1Venkar Chemicals
06 2Arch Pharmalabs
07 2Aurobindo Pharma Limited
08 1Aurore Life Sciences
09 3Cipla
10 1Curia
11 1DEAFARMA
12 1Derivados Quimicos SAU
13 1Dr. Raju’s Pharma Solutions
14 1Esteve Quimica
15 1H. Lundbeck AS
16 2Hetero Drugs
17 1Heumann
18 1Ipca Laboratories
19 1Jiangsu Jiwa Rintech Pharmaceutical
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21 2Jubilant Generics
22 2Jubilant Pharmova
23 1Kekule Pharma
24 1Mahban Group
25 1Natco Pharma
26 1Nishchem International Pvt. Ltd
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29 1Smilax Laboratories Limited
30 1Sumitomo Chemical
31 2Sun Pharmaceutical Industries Limited
32 1Synergene Active Ingredients Pvt Ltd
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01 4China
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01 16Active
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01 14Valid
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01 1WC-0014
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03 1WC-0066
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05 1WC-0092
06 1WC-0119
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01 147621-022
02 151686-0007
03 155486-1572
04 159349-0010
05 163850-3616
06 164220-105
07 165015-721
08 165372-1101
09 165372-1130
10 165862-336
11 165977-0018
12 165977-0053
13 172761-006
14 184206-0022
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-12-17
Pay. Date : 2023-06-05
DMF Number : 36925
Submission : 2023-05-22
Status : Active
Type : II
Certificate Number : R0-CEP 2021-437 - Rev 00
Issue Date : 2023-08-29
Type : Chemical
Substance Number : 2288
Status : Valid
NDC Package Code : 51686-0007
Start Marketing Date : 2024-01-03
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 : 23979
Submission : 2010-07-19
Status : Active
Type : II
Certificate Number : R1-CEP 2011-214 - Rev 00
Issue Date : 2017-09-14
Type : Chemical
Substance Number : 2288
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16788
Submission : 2003-08-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20094
Submission : 2006-12-06
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17104
Submission : 2004-01-13
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17511
Submission : 2004-07-01
Status : Inactive
Type : II
98
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A Lupram manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lupram, including repackagers and relabelers. The FDA regulates Lupram manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lupram 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 Lupram supplier is an individual or a company that provides Lupram active pharmaceutical ingredient (API) or Lupram finished formulations upon request. The Lupram suppliers may include Lupram API manufacturers, exporters, distributors and traders.
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We have 37 companies offering Lupram
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