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Metoclopramide - 68788-0430-3 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 68788-0430
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: 68788-0430
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070184
Marketing Category: ANDA
Start Marketing Date: 20130401

Package Information of Metoclopramide

Package NDC: 68788-0430-3
Package Description: 30 TABLET in 1 BOTTLE (68788-0430-3)

NDC Information of Metoclopramide

NDC Code 68788-0430-3
Proprietary Name Metoclopramide
Package Description 30 TABLET in 1 BOTTLE (68788-0430-3)
Product NDC 68788-0430
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130401
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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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