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Metoclopramide - 49884-685-05 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 49884-685
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: 49884-685
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070581
Marketing Category: ANDA
Start Marketing Date: 19851017

Package Information of Metoclopramide

Package NDC: 49884-685-05
Package Description: 500 TABLET in 1 BOTTLE (49884-685-05)

NDC Information of Metoclopramide

NDC Code 49884-685-05
Proprietary Name Metoclopramide
Package Description 500 TABLET in 1 BOTTLE (49884-685-05)
Product NDC 49884-685
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 Par Pharmaceutical Inc.
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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