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Metoclopramide - 42769-1394-5 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide

Product NDC: 42769-1394
Proprietary Name: Metoclopramide
Non Proprietary Name: Metoclopramide Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Metoclopramide Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metoclopramide

Product NDC: 42769-1394
Labeler Name: BayPharma Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA017854
Marketing Category: ANDA
Start Marketing Date: 20100215

Package Information of Metoclopramide

Package NDC: 42769-1394-5
Package Description: 500 TABLET in 1 BOTTLE, PLASTIC (42769-1394-5)

NDC Information of Metoclopramide

NDC Code 42769-1394-5
Proprietary Name Metoclopramide
Package Description 500 TABLET in 1 BOTTLE, PLASTIC (42769-1394-5)
Product NDC 42769-1394
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100215
Marketing Category Name ANDA
Labeler Name BayPharma Inc.
Substance Name METOCLOPRAMIDE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]

Complete Information of Metoclopramide


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