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Metoclopramide - 0093-2203-01 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 0093-2203
Proprietary Name: Metoclopramide
Non Proprietary Name: Metoclopramide
Active Ingredient(s): 10    mg/1 & nbsp;   Metoclopramide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metoclopramide

Product NDC: 0093-2203
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070184
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Metoclopramide

Package NDC: 0093-2203-01
Package Description: 100 TABLET in 1 BOTTLE (0093-2203-01)

NDC Information of Metoclopramide

NDC Code 0093-2203-01
Proprietary Name Metoclopramide
Package Description 100 TABLET in 1 BOTTLE (0093-2203-01)
Product NDC 0093-2203
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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


General Information