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Metoclopramide - 51079-283-19 - (Metoclopramide)

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Drug Information of Metoclopramide

Product NDC: 51079-283
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: 51079-283
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070184
Marketing Category: ANDA
Start Marketing Date: 20110823

Package Information of Metoclopramide

Package NDC: 51079-283-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-283-19) > 1 TABLET in 1 BLISTER PACK (51079-283-17)

NDC Information of Metoclopramide

NDC Code 51079-283-19
Proprietary Name Metoclopramide
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-283-19) > 1 TABLET in 1 BLISTER PACK (51079-283-17)
Product NDC 51079-283
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoclopramide
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110823
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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