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Metoclopramide Hydrochloride - 63739-482-10 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide Hydrochloride

Product NDC: 63739-482
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: 63739-482
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078374
Marketing Category: ANDA
Start Marketing Date: 20110822

Package Information of Metoclopramide Hydrochloride

Package NDC: 63739-482-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-482-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Metoclopramide Hydrochloride

NDC Code 63739-482-10
Proprietary Name Metoclopramide Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-482-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-482
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110822
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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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