Metoclopramide

Product NDC
63629-8745
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Metoclopramide
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA070184
Marketing category
ANDA
Substance
METOCLOPRAMIDE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
63629-8745-1500 TABLET in 1 BOTTLE (63629-8745-1) 1990-09-30NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
MetoclopramideBryant Ranch Prepack2024-01-11HUMAN PRESCRIPTION DRUG LABEL103