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Metoclopramide - 0121-0576-16 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide

Product NDC: 0121-0576
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: 0121-0576
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072744
Marketing Category: ANDA
Start Marketing Date: 19910601

Package Information of Metoclopramide

Package NDC: 0121-0576-16
Package Description: 473 mL in 1 BOTTLE (0121-0576-16)

NDC Information of Metoclopramide

NDC Code 0121-0576-16
Proprietary Name Metoclopramide
Package Description 473 mL in 1 BOTTLE (0121-0576-16)
Product NDC 0121-0576
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19910601
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, 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


General Information