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Metoclopramide - 55154-5510-0 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 55154-5510
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: 55154-5510
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070184
Marketing Category: ANDA
Start Marketing Date: 20110823

Package Information of Metoclopramide

Package NDC: 55154-5510-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5510-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Metoclopramide

NDC Code 55154-5510-0
Proprietary Name Metoclopramide
Package Description 10 BLISTER PACK in 1 BAG (55154-5510-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110823
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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