MedPath

Metoclopramide

Rx only

Approved
Approval ID

50a3cf38-66dc-4fa5-8a45-adf959c987ab

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Nov 10, 2023

Manufacturers
FDA

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

DUNS: 780779901

Products 1

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

Metoclopramide Hydrochloride

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code23155-240
Application NumberANDA204756
Product Classification
M
Marketing Category
C73584
G
Generic Name
Metoclopramide Hydrochloride
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateJanuary 25, 2022
FDA Product Classification

INGREDIENTS (5)

METOCLOPRAMIDE HYDROCHLORIDEActive
Quantity: 5 mg in 1 mL
Code: W1792A2RVD
Classification: ACTIM
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Metoclopramide - FDA Drug Approval Details