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Metoclopramide - 0228-2269-10 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 0228-2269
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: 0228-2269
Labeler Name: Actavis Elizabeth LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070581
Marketing Category: ANDA
Start Marketing Date: 19851017

Package Information of Metoclopramide

Package NDC: 0228-2269-10
Package Description: 100 TABLET in 1 BOTTLE (0228-2269-10)

NDC Information of Metoclopramide

NDC Code 0228-2269-10
Proprietary Name Metoclopramide
Package Description 100 TABLET in 1 BOTTLE (0228-2269-10)
Product NDC 0228-2269
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19851017
Marketing Category Name ANDA
Labeler Name Actavis Elizabeth 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


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