DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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01 2Dr. Reddy's Laboratories
02 1Shandong Loncom Pharmaceutical
03 1Sumar Biotech
04 1Alembic Pharmaceuticals Limited
05 1Chongqing Carelife Pharmaceutical
06 1Eisai
07 1Guangzhou Tosun Pharmaceutical
08 1Hetero Drugs
09 2MSN Laboratories
10 1Mac-Chem Products (India) Pvt.Ltd
11 1Natco Pharma
12 2Olon S.p.A
13 1Parsian Pharamceutical
14 1Shanghai Hope Chem
15 1Shilpa Medicare
16 1Sichuan Qingmu Pharmaceutical
17 1Sun Pharmaceutical Industries Limited
18 1Vannsh Life Sciences
19 1Yangtze River Pharmaceutical Group
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01 6China
02 12India
03 1Iran
04 2Italy
05 1Japan
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01 10Active
02 12Blank
01 22Blank
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01 22Blank
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01 1WC-0039
02 1WC-0067
03 1WC-0349
04 1WC-0349A5-A6
05 1WC-0372
06 17Blank
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01 1No. 3834-5-ND
02 1No. 574-26-ND
03 1No. 674-4-ND
04 1No. 674-4-ND(A)
05 18Blank
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01 117337-0099
02 117337-0314
03 154893-0077
04 154893-0112
05 171796-005
06 182920-036
07 16Blank
01 22Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-10-24
Pay. Date : 2018-08-09
DMF Number : 32905
Submission : 2018-06-26
Status : Active
Type : II
Date of Issue : 2022-06-06
Valid Till : 2025-07-07
Written Confirmation Number : WC-0039
Address of the Firm :
NDC Package Code : 71796-005
Start Marketing Date : 2018-06-26
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Pami Future Co., Ltd.
Registration Date : 2024-10-25
Registration Number : No. 574-26-ND
Manufacturer Name : Dr. Reddy's Laboratories Limited
Manufacturer Address : CTO Unit-VI, APIIC Industrial Estate, Pydibhimavaram Village, Ranasthalam Mandal, Srikakulam District, Andhra Pradesh - 532 409, India
Available Reg Filing : BR |
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-11-30
Pay. Date : 2021-11-08
DMF Number : 36031
Submission : 2021-06-30
Status : Active
Type : II
Date of Issue : 2022-06-17
Valid Till : 2025-07-07
Written Confirmation Number : WC-0067
Address of the Firm :
Available Reg Filing : BR |
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-11-20
Pay. Date : 2018-09-04
DMF Number : 33083
Submission : 2018-09-04
Status : Active
Type : II
NDC Package Code : 82920-036
Start Marketing Date : 2022-08-15
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 : 39887
Submission : 2024-04-30
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-01-24
Pay. Date : 2021-12-16
DMF Number : 36197
Submission : 2021-12-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 33964
Submission : 2019-06-27
Status : Active
Type : II
NDC Package Code : 17337-0314
Start Marketing Date : 2022-05-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-11-26
Pay. Date : 2024-09-30
DMF Number : 37347
Submission : 2022-07-28
Status : Active
Type : II
NDC Package Code : 17337-0099
Start Marketing Date : 2021-10-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-03-27
Pay. Date : 2018-12-12
DMF Number : 33331
Submission : 2019-02-04
Status : Active
Type : II
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PharmaCompass offers a list of Lenvatinib Mesylate 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 Lenvatinib Mesylate manufacturer or Lenvatinib Mesylate supplier for your needs.
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A Lenvatinib Mesylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lenvatinib Mesylate, including repackagers and relabelers. The FDA regulates Lenvatinib Mesylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lenvatinib Mesylate 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 Lenvatinib Mesylate supplier is an individual or a company that provides Lenvatinib Mesylate active pharmaceutical ingredient (API) or Lenvatinib Mesylate finished formulations upon request. The Lenvatinib Mesylate suppliers may include Lenvatinib Mesylate API manufacturers, exporters, distributors and traders.
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We have 19 companies offering Lenvatinib Mesylate
Get in contact with the supplier of your choice: