Reglan - 0091-6701-70 - (metoclopramide hydrochloride)

Alphabetical Index


Drug Information of Reglan

Product NDC: 0091-6701
Proprietary Name: Reglan
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 Reglan

Product NDC: 0091-6701
Labeler Name: UCB, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017854
Marketing Category: NDA
Start Marketing Date: 20030505

Package Information of Reglan

Package NDC: 0091-6701-70
Package Description: 500 TABLET in 1 BOTTLE (0091-6701-70)

NDC Information of Reglan

NDC Code 0091-6701-70
Proprietary Name Reglan
Package Description 500 TABLET in 1 BOTTLE (0091-6701-70)
Product NDC 0091-6701
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoclopramide hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030505
Marketing Category Name NDA
Labeler Name UCB, 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 Reglan


General Information