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Metoclopramide - 60432-622-16 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide

Product NDC: 60432-622
Proprietary Name: Metoclopramide
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

Product NDC: 60432-622
Labeler Name: Morton Grove Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074703
Marketing Category: ANDA
Start Marketing Date: 19950405

Package Information of Metoclopramide

Package NDC: 60432-622-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC (60432-622-16)

NDC Information of Metoclopramide

NDC Code 60432-622-16
Proprietary Name Metoclopramide
Package Description 473 mL in 1 BOTTLE, PLASTIC (60432-622-16)
Product NDC 60432-622
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19950405
Marketing Category Name ANDA
Labeler Name Morton Grove Pharmaceuticals, 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


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