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METOCLOPRAMIDE - 16590-151-60 - (METOCLOPRAMIDE HYDROCHLORIDE)

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Drug Information of METOCLOPRAMIDE

Product NDC: 16590-151
Proprietary Name: METOCLOPRAMIDE
Non Proprietary Name: METOCLOPRAMIDE HYDROCHLORIDE
Active Ingredient(s): 10    mg/1 & nbsp;   METOCLOPRAMIDE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of METOCLOPRAMIDE

Product NDC: 16590-151
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077878
Marketing Category: ANDA
Start Marketing Date: 20060828

Package Information of METOCLOPRAMIDE

Package NDC: 16590-151-60
Package Description: 60 TABLET in 1 BOTTLE (16590-151-60)

NDC Information of METOCLOPRAMIDE

NDC Code 16590-151-60
Proprietary Name METOCLOPRAMIDE
Package Description 60 TABLET in 1 BOTTLE (16590-151-60)
Product NDC 16590-151
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METOCLOPRAMIDE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060828
Marketing Category Name ANDA
Labeler Name STAT RX USA 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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