Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
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01 1Malladi Drugs & Pharmaceuticals Limited
02 1LGM Pharma
03 1Evonik
04 1Nuray Chemicals Private Limited
05 1HRV Global Life Sciences
06 1Tenatra Chemie
07 1TAPI Technology & API Services
08 1Biotechnica DWC
09 1Cambrex Corporation
10 1Centaur Pharmaceuticals
11 1Cipla
12 1Enovachem Pharmaceutical
13 1F.I.S. Fabbrica Italiana Sintetici
14 1Fagron Group
15 1Formil Quimica Ltd
16 1Global Calcium
17 1IIQUIAP
18 1Kalintis Healthcare
19 1Lake Chemicals
20 1Letco Medical
21 1Nishchem International Pvt. Ltd
22 2Pcca
23 3R L Fine Chem
24 1Sandoz B2B
25 1Spectrum Chemical
26 1Srini Pharmaceuticals
27 1Sun Pharmaceutical Industries Limited
28 1Blank
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01 1Algeria
02 1Brazil
03 1Germany
04 15India
05 1Israel
06 1Italy
07 1Mexico
08 1Netherlands
09 1Switzerland
10 5U.S.A
11 2United Kingdom
12 1Blank
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01 7Active
02 5Inactive
03 19Blank
01 6Valid
02 25Blank
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01 1217MF10849
02 1218MF10781
03 29Blank
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01 1WC-0093
02 1WC-0101
03 1WC-0107
04 1WC-0139
05 1WC-0445A2
06 1WC-0445A3
07 25Blank
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01 31Blank
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01 112828-0025
02 148087-0076
03 149452-4140
04 151552-0729
05 151927-0195
06 151927-1005
07 152696-0002
08 157218-950
09 158159-103
10 162991-1682
11 171554-009
12 172166-001
13 176420-296
14 18Blank
01 31Blank
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23247
Submission : 2009-11-05
Status : Active
Type : II
Date of Issue : 2022-06-08
Valid Till : 2025-07-14
Written Confirmation Number : WC-0093
Address of the Firm :
NDC Package Code : 57218-950
Start Marketing Date : 2009-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5041
Submission : 1983-07-09
Status : Active
Type : II
Certificate Number : R1-CEP 2008-142 - Rev 04
Issue Date : 2021-03-30
Type : Chemical
Substance Number : 1121
Status : Valid
NDC Package Code : 52696-0002
Start Marketing Date : 1983-07-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
NDC Package Code : 58159-103
Start Marketing Date : 2024-08-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (35kg/35kg)
Marketing Category : BULK INGREDIENT
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19268
Submission : 2006-03-21
Status : Inactive
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-01-29
Pay. Date : 2020-12-08
DMF Number : 35299
Submission : 2020-12-11
Status : Active
Type : II
NDC Package Code : 72166-001
Start Marketing Date : 2018-04-09
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 : 15156
Submission : 2000-11-21
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5747
Submission : 1985-03-13
Status : Inactive
Type : II
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PharmaCompass offers a list of Lorazepam 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 Lorazepam manufacturer or Lorazepam supplier for your needs.
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A Lorsilan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lorsilan, including repackagers and relabelers. The FDA regulates Lorsilan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lorsilan 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 Lorsilan supplier is an individual or a company that provides Lorsilan active pharmaceutical ingredient (API) or Lorsilan finished formulations upon request. The Lorsilan suppliers may include Lorsilan API manufacturers, exporters, distributors and traders.
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We have 27 companies offering Lorsilan
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