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Metoclopramide - 63304-845-30 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 63304-845
Proprietary Name: Metoclopramide
Non Proprietary Name: Metoclopramide
Active Ingredient(s): 5    mg/1 & nbsp;   Metoclopramide
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metoclopramide

Product NDC: 63304-845
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078807
Marketing Category: ANDA
Start Marketing Date: 20090313

Package Information of Metoclopramide

Package NDC: 63304-845-30
Package Description: 30 TABLET in 1 BOTTLE (63304-845-30)

NDC Information of Metoclopramide

NDC Code 63304-845-30
Proprietary Name Metoclopramide
Package Description 30 TABLET in 1 BOTTLE (63304-845-30)
Product NDC 63304-845
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090313
Marketing Category Name ANDA
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name METOCLOPRAMIDE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]

Complete Information of Metoclopramide


General Information