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Metoclopramide - 63629-1618-3 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 63629-1618
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: 63629-1618
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078807
Marketing Category: ANDA
Start Marketing Date: 20090313

Package Information of Metoclopramide

Package NDC: 63629-1618-3
Package Description: 60 TABLET in 1 BOTTLE (63629-1618-3)

NDC Information of Metoclopramide

NDC Code 63629-1618-3
Proprietary Name Metoclopramide
Package Description 60 TABLET in 1 BOTTLE (63629-1618-3)
Product NDC 63629-1618
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090313
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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