01 1Aurobindo Pharma Limited
02 1MSN Laboratories Private Limited
01 1Lorcaserin Hydrochloride
02 1Lorcaserin Hydrochloride Hemihydrate
01 2India
LORCASERIN HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 59651-017
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
LORCASERIN HYDROCHLORIDE HEMIHYDRATE
NDC Package Code : 14501-0023
Start Marketing Date : 2015-04-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A LORCASERIN HYDROCHLORIDE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of LORCASERIN HYDROCHLORIDE, including repackagers and relabelers. The FDA regulates LORCASERIN HYDROCHLORIDE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. LORCASERIN HYDROCHLORIDE 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 LORCASERIN HYDROCHLORIDE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A LORCASERIN HYDROCHLORIDE supplier is an individual or a company that provides LORCASERIN HYDROCHLORIDE active pharmaceutical ingredient (API) or LORCASERIN HYDROCHLORIDE finished formulations upon request. The LORCASERIN HYDROCHLORIDE suppliers may include LORCASERIN HYDROCHLORIDE API manufacturers, exporters, distributors and traders.
click here to find a list of LORCASERIN HYDROCHLORIDE 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 LORCASERIN HYDROCHLORIDE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for LORCASERIN HYDROCHLORIDE 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 LORCASERIN HYDROCHLORIDE 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 LORCASERIN HYDROCHLORIDE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a LORCASERIN HYDROCHLORIDE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of LORCASERIN HYDROCHLORIDE suppliers with NDC on PharmaCompass.
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