Veranova: A CDMO that manages complexity with confidence.
01 1Veranova
02 3Dr. Reddy's Laboratories
03 1Alembic Pharmaceuticals Limited
04 1Aurobindo Pharma Limited
05 1Biocon
06 1Changzhou Pharmaceutical Factory
07 2Cipla
08 1Deva Holding AS
09 1Hetero Drugs
10 1Kyongbo Pharmaceutical Co., Ltd
11 2MSN Laboratories
12 1Reliance Life Sciences Private Limited
13 1Shandong Anhong Pharmaceutical
14 1Shilpa Medicare
15 1Sun Pharmaceutical Industries Limited
16 1Synthon Pharmaceuticals
17 1Viatris
18 1Yangtze River Pharmaceutical Group
19 1Zydus Lifesciences
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : Complete
Rev. Date : 2022-07-26
Pay. Date : 2022-05-10
DMF Number : 36810
Submission : 2022-05-12
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29690
Submission : 2015-09-30
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : Complete
Rev. Date : 2015-12-09
Pay. Date : 2015-09-28
DMF Number : 29691
Submission : 2015-09-30
Status :
Type : II
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35505
Submission : 2020-12-31
Status :
Type : II
97
PharmaCompass offers a list of Lenalidomide 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 Lenalidomide manufacturer or Lenalidomide supplier for your needs.
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A ALBB-015321 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ALBB-015321, including repackagers and relabelers. The FDA regulates ALBB-015321 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ALBB-015321 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 ALBB-015321 supplier is an individual or a company that provides ALBB-015321 active pharmaceutical ingredient (API) or ALBB-015321 finished formulations upon request. The ALBB-015321 suppliers may include ALBB-015321 API manufacturers, exporters, distributors and traders.
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A ALBB-015321 DMF (Drug Master File) is a document detailing the whole manufacturing process of ALBB-015321 active pharmaceutical ingredient (API) in detail. Different forms of ALBB-015321 DMFs exist exist since differing nations have different regulations, such as ALBB-015321 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A ALBB-015321 DMF submitted to regulatory agencies in the US is known as a USDMF. ALBB-015321 USDMF includes data on ALBB-015321's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The ALBB-015321 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 19 companies offering ALBB-015321
Get in contact with the supplier of your choice:
