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Metoclopramide Hydrochloride - 68788-9706-3 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide Hydrochloride

Product NDC: 68788-9706
Proprietary Name: Metoclopramide Hydrochloride
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 Hydrochloride

Product NDC: 68788-9706
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071250
Marketing Category: ANDA
Start Marketing Date: 20130206

Package Information of Metoclopramide Hydrochloride

Package NDC: 68788-9706-3
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (68788-9706-3)

NDC Information of Metoclopramide Hydrochloride

NDC Code 68788-9706-3
Proprietary Name Metoclopramide Hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (68788-9706-3)
Product NDC 68788-9706
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130206
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 Hydrochloride


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