01 1HETERO DRUGS LIMITED
02 1Hetero Drugs Limited
01 1Lercanidipine Hydrochloride
02 1Lercanidipine Hydrochloride (Form-I)
01 2India
NDC Package Code : 65977-0099
Start Marketing Date : 2013-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0136
Start Marketing Date : 2004-06-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Lercanidipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lercanidipine, including repackagers and relabelers. The FDA regulates Lercanidipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lercanidipine 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 Lercanidipine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lercanidipine supplier is an individual or a company that provides Lercanidipine active pharmaceutical ingredient (API) or Lercanidipine finished formulations upon request. The Lercanidipine suppliers may include Lercanidipine API manufacturers, exporters, distributors and traders.
click here to find a list of Lercanidipine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Lercanidipine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Lercanidipine API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Lercanidipine as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Lercanidipine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lercanidipine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Lercanidipine suppliers with NDC on PharmaCompass.
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