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Metoclopramide - 53808-0722-1 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 53808-0722
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: 53808-0722
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071250
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Metoclopramide

Package NDC: 53808-0722-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0722-1)

NDC Information of Metoclopramide

NDC Code 53808-0722-1
Proprietary Name Metoclopramide
Package Description 30 TABLET in 1 BLISTER PACK (53808-0722-1)
Product NDC 53808-0722
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
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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