Metoclopramide

Approved

Approval ID

79754097-4514-297e-e053-2991aa0a4804

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

May 23, 2023

Manufacturers

FDA

Medical Purchasing Solutions, LLC

DUNS: 601458529

Products 1

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

NDC Product Code71872-7076

Application NumberANDA073118

Marketing CategoryC73584

Route of AdministrationINTRAMUSCULAR, INTRAVENOUS

Effective DateMay 23, 2023

Generic Namemetoclopramide

SODIUM CHLORIDEInactive

Quantity: 8.5 mg in 1 mL

Code: 451W47IQ8X

Classification: IACT

HYDROCHLORIC ACIDInactive

Code: QTT17582CB

Classification: IACT

WATERInactive

Code: 059QF0KO0R

Classification: IACT

SODIUM HYDROXIDEInactive

Code: 55X04QC32I

Classification: IACT

METOCLOPRAMIDE HYDROCHLORIDEActive

Quantity: 5 mg in 1 mL

Code: W1792A2RVD

Classification: ACTIM