Metoclopramide

Metoclopramide Injection, USP Rx only

Approved

Approval ID

cccf04bd-7463-40b8-a41f-cb1093c358d7

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Jan 31, 2022

Manufacturers

FDA

Teva Parenteral Medicines, Inc.

DUNS: 794362533

Products 1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code0703-4502

Application NumberANDA073135

Marketing CategoryC73584

Route of AdministrationINTRAMUSCULAR, INTRAVENOUS

Effective DateJanuary 31, 2022

Generic NameMetoclopramide

METOCLOPRAMIDE HYDROCHLORIDEActive

Quantity: 5 mg in 1 mL

Code: W1792A2RVD

Classification: ACTIM

SODIUM CHLORIDEInactive

Code: 451W47IQ8X

Classification: IACT

WATERInactive

Code: 059QF0KO0R

Classification: IACT

HYDROCHLORIC ACIDInactive

Code: QTT17582CB

Classification: IACT

SODIUM HYDROXIDEInactive

Code: 55X04QC32I

Classification: IACT