01 1COSMA Spa
02 1Fagron Inc.
03 1Fagron Services BV
04 1Icrom S.r.l.
05 2Ipca Laboratories Limited
06 1Lundbeck Pharmaceuticals Italy S.p.A.
07 1Professional Compounding Centers of America
08 1Professional Compounding Centers of America dba PCCA
01 2METOCLOPRAMIDE HYDROCHLORIDE
02 1METOCLOPRAMIDE HYDROCHLORIDE MONOHYDRATE
03 6Metoclopramide Hydrochloride
01 1Denmark
02 2India
03 2Italy
04 2Netherlands
05 2United Kingdom
NDC Package Code : 51604-0005
Start Marketing Date : 2009-10-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1549
Start Marketing Date : 2018-01-12
End Marketing Date : 2027-01-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 76003-0739
Start Marketing Date : 2018-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 45562-1737
Start Marketing Date : 1998-01-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 40700-0010
Start Marketing Date : 2020-02-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1119
Start Marketing Date : 2012-06-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1139
Start Marketing Date : 2012-03-18
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0185
Start Marketing Date : 2012-04-16
End Marketing Date : 2028-07-07
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1082
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Metoclopramide Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Metoclopramide Hydrochloride, including repackagers and relabelers. The FDA regulates Metoclopramide Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Metoclopramide 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 Metoclopramide Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Metoclopramide Hydrochloride supplier is an individual or a company that provides Metoclopramide Hydrochloride active pharmaceutical ingredient (API) or Metoclopramide Hydrochloride finished formulations upon request. The Metoclopramide Hydrochloride suppliers may include Metoclopramide Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Metoclopramide 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 Metoclopramide Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Metoclopramide 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 Metoclopramide 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 Metoclopramide Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Metoclopramide Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Metoclopramide Hydrochloride suppliers with NDC on PharmaCompass.
We have 6 companies offering Metoclopramide Hydrochloride
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