Maithri Drugs: Dedicated to your API needs.
01 2Maithri Drugs
01 1LERCANIDIPINE HYDROCHLORIDE (AMORPHOUS)
02 1LERCANIDIPINE HYDROCHLORIDE (FORM-I)
01 2India
01 2Active
01 2Blank
Maithri Drugs: Dedicated to your API needs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35507
Submission : 2020-12-30
Status : Active
Type : II
Maithri Drugs: Dedicated to your API needs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 35609
Submission : 2021-01-30
Status : Active
Type : II
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PharmaCompass offers a list of Lercanidipine Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Lercanidipine Hydrochloride manufacturer or Lercanidipine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lercanidipine Hydrochloride manufacturer or Lercanidipine Hydrochloride supplier.
A Lerkamen manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lerkamen, including repackagers and relabelers. The FDA regulates Lerkamen manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lerkamen API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Lerkamen manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Lerkamen supplier is an individual or a company that provides Lerkamen active pharmaceutical ingredient (API) or Lerkamen finished formulations upon request. The Lerkamen suppliers may include Lerkamen API manufacturers, exporters, distributors and traders.
click here to find a list of Lerkamen suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Lerkamen DMF (Drug Master File) is a document detailing the whole manufacturing process of Lerkamen active pharmaceutical ingredient (API) in detail. Different forms of Lerkamen DMFs exist exist since differing nations have different regulations, such as Lerkamen USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Lerkamen DMF submitted to regulatory agencies in the US is known as a USDMF. Lerkamen USDMF includes data on Lerkamen's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Lerkamen USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Lerkamen suppliers with USDMF on PharmaCompass.
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