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Metoclopramide Hydrochloride - 66689-031-50 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide Hydrochloride

Product NDC: 66689-031
Proprietary Name: Metoclopramide Hydrochloride
Non Proprietary Name: Metoclopramide Hydrochloride
Active Ingredient(s): 5    mg/5mL & nbsp;   Metoclopramide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Metoclopramide Hydrochloride

Product NDC: 66689-031
Labeler Name: VistaPharm Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075051
Marketing Category: ANDA
Start Marketing Date: 20100212

Package Information of Metoclopramide Hydrochloride

Package NDC: 66689-031-50
Package Description: 5 TRAY in 1 CASE (66689-031-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-031-01)

NDC Information of Metoclopramide Hydrochloride

NDC Code 66689-031-50
Proprietary Name Metoclopramide Hydrochloride
Package Description 5 TRAY in 1 CASE (66689-031-50) > 10 CUP, UNIT-DOSE in 1 TRAY > 10 mL in 1 CUP, UNIT-DOSE (66689-031-01)
Product NDC 66689-031
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20100212
Marketing Category Name ANDA
Labeler Name VistaPharm Inc.
Substance Name METOCLOPRAMIDE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]

Complete Information of Metoclopramide Hydrochloride


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