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Metoclopramide Hydrochloride - 16714-062-01 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide Hydrochloride

Product NDC: 16714-062
Proprietary Name: Metoclopramide Hydrochloride
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 Hydrochloride

Product NDC: 16714-062
Labeler Name: Northstar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078374
Marketing Category: ANDA
Start Marketing Date: 20110317

Package Information of Metoclopramide Hydrochloride

Package NDC: 16714-062-01
Package Description: 30 TABLET in 1 BOTTLE (16714-062-01)

NDC Information of Metoclopramide Hydrochloride

NDC Code 16714-062-01
Proprietary Name Metoclopramide Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (16714-062-01)
Product NDC 16714-062
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110317
Marketing Category Name ANDA
Labeler Name Northstar RxLLC
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 Hydrochloride


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