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Metoclopramide - 54569-0434-0 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 54569-0434
Proprietary Name: Metoclopramide
Non Proprietary Name: Metoclopramide
Active Ingredient(s): 10    mg/1 & nbsp;   Metoclopramide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metoclopramide

Product NDC: 54569-0434
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070184
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Metoclopramide

Package NDC: 54569-0434-0
Package Description: 30 TABLET in 1 BOTTLE (54569-0434-0)

NDC Information of Metoclopramide

NDC Code 54569-0434-0
Proprietary Name Metoclopramide
Package Description 30 TABLET in 1 BOTTLE (54569-0434-0)
Product NDC 54569-0434
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name METOCLOPRAMIDE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]

Complete Information of Metoclopramide


General Information