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