Metoclopramide

Product NDC

50436-1873

11-digit product format

504361873

Labeler code

50436

Product ID

50436-1873_623fb153-dde3-46f2-a170-2aed4163c83c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metoclopramide

Dosage form

TABLET

Route

ORAL

Labeler

Unit Dose Services

Application

ANDA072801

Marketing category

ANDA

Marketing start

1993-07-01

Marketing end

0000-00-00

Substance

METOCLOPRAMIDE HYDROCHLORIDE

Active strength

5 mg/1

Pharmacologic classes

Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record