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Metoclopramide Hydrochloride - 0591-2228-01 - (Metoclopramide Hydrochloride)

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Drug Information of Metoclopramide Hydrochloride

Product NDC: 0591-2228
Proprietary Name: Metoclopramide Hydrochloride
Non Proprietary Name: Metoclopramide Hydrochloride
Active Ingredient(s): 5    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: 0591-2228
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072750
Marketing Category: ANDA
Start Marketing Date: 20081223

Package Information of Metoclopramide Hydrochloride

Package NDC: 0591-2228-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0591-2228-01)

NDC Information of Metoclopramide Hydrochloride

NDC Code 0591-2228-01
Proprietary Name Metoclopramide Hydrochloride
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0591-2228-01)
Product NDC 0591-2228
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081223
Marketing Category Name ANDA
Labeler Name Watson Laboratories, 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 Hydrochloride


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