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Metoclopramide - 52125-122-02 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 52125-122
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: 52125-122
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078807
Marketing Category: ANDA
Start Marketing Date: 20130314

Package Information of Metoclopramide

Package NDC: 52125-122-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-122-02)

NDC Information of Metoclopramide

NDC Code 52125-122-02
Proprietary Name Metoclopramide
Package Description 30 TABLET in 1 BLISTER PACK (52125-122-02)
Product NDC 52125-122
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130314
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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