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Metoclopramide - 55154-0452-5 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide

Product NDC: 55154-0452
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: 55154-0452
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017862
Marketing Category: NDA
Start Marketing Date: 20101209

Package Information of Metoclopramide

Package NDC: 55154-0452-5
Package Description: 5 VIAL, SINGLE-DOSE in 1 BAG (55154-0452-5) > 2 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Metoclopramide

NDC Code 55154-0452-5
Proprietary Name Metoclopramide
Package Description 5 VIAL, SINGLE-DOSE in 1 BAG (55154-0452-5) > 2 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55154-0452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20101209
Marketing Category Name NDA
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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