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Metoclopramide - 0615-7752-39 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 0615-7752
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: 0615-7752
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070581
Marketing Category: ANDA
Start Marketing Date: 19851017

Package Information of Metoclopramide

Package NDC: 0615-7752-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7752-39)

NDC Information of Metoclopramide

NDC Code 0615-7752-39
Proprietary Name Metoclopramide
Package Description 30 TABLET in 1 BLISTER PACK (0615-7752-39)
Product NDC 0615-7752
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 NCS HealthCare of KY, Inc dba Vangard Labs
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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