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Metoclopramide - 55154-2353-5 - (METOCLOPRAMIDE HYDROCHLORIDE)

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Drug Information of Metoclopramide

Product NDC: 55154-2353
Proprietary Name: Metoclopramide
Non Proprietary Name: METOCLOPRAMIDE HYDROCHLORIDE
Active Ingredient(s): 5    mg/mL & nbsp;   METOCLOPRAMIDE HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Metoclopramide

Product NDC: 55154-2353
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073118
Marketing Category: ANDA
Start Marketing Date: 20090922

Package Information of Metoclopramide

Package NDC: 55154-2353-5
Package Description: 5 VIAL in 1 BAG (55154-2353-5) > 2 mL in 1 VIAL

NDC Information of Metoclopramide

NDC Code 55154-2353-5
Proprietary Name Metoclopramide
Package Description 5 VIAL in 1 BAG (55154-2353-5) > 2 mL in 1 VIAL
Product NDC 55154-2353
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METOCLOPRAMIDE HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20090922
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name METOCLOPRAMIDE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]

Complete Information of Metoclopramide


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