NDC 0703-4502-01 - Metoclopramide

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 0703-4502
Requested NDC: 0703-4502-01
Package NDCs from labels: 0703-4502-01, 0703-4502-04, 0703-4502-91, 0703-4502-93, 0703-4502-81, 0703-4502-84
Manufacturer: Cardinal Health 107, LLC
Effective date: 2026-09-10
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Metoclopramide - Cardinal Health 107, LLC	Cardinal Health 107, LLC	2026-09-10	HUMAN PRESCRIPTION DRUG LABEL
Metoclopramide Injection, USP Rx only	Teva Parenteral Medicines, Inc.	2026-04-22	HUMAN PRESCRIPTION DRUG LABEL
Metoclopramide Injection, USP Rx only	Teva Parenteral Medicines, Inc.	2026-04-15	HUMAN PRESCRIPTION DRUG LABEL
Metoclopramide - Medical Purchasing Solutions, LLC	Medical Purchasing Solutions, LLC	2020-01-24	HUMAN PRESCRIPTION DRUG LABEL
Metoclopramide Injection USP 4502 Rx only	Teva Parenteral Medicines, Inc.	2015-05-01	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
0703-4502-01	Metoclopramide	2 mL in 1 VIAL, SINGLE-USE	INJECTION, SOLUTION	2	14
0703-4502-04	Metoclopramide	25 in 1 TRAY	INJECTION, SOLUTION	25	14
0703-4502-91	Metoclopramide	2 mL in 1 VIAL, SINGLE-USE	INJECTION, SOLUTION	2	8
0703-4502-93	Metoclopramide	10 in 1 CARTON	INJECTION, SOLUTION	10	8

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0703-4502	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	13	Current NDC, Legacy NDC, 2 package rows	20230628_cccf04bd-7463-40b8-a41f-cb1093c358d7.zip
0703-4502	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	7	Current NDC, Legacy NDC, 2 package rows	20240906_5645a752-8868-4b51-8b59-48bb4276d763.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0703-4502-01	ML - Milliliter	0703-4502	3c2e19db-3873-43d2-9b74-efb5910a9860	1	2014-02-04
0703-4502-04	ML - Milliliter	0703-4502	970d311d-0e29-4d91-9b8a-561465ea9a7a	1	2014-01-04
0703-4502-81	ML - Milliliter	0703-4502	d8a195ab-53f6-411d-a01e-45b69b4e4f51	1	2015-09-10
0703-4502-84	ML - Milliliter	0703-4502	b74cc0a4-bfb8-499f-90fb-225c8939f713	1	2015-09-10
0703-4502-91	ML - Milliliter	0703-4502	c422a339-78a6-4e65-9e5c-d13779f4857a	1	2015-03-03
0703-4502-93	ML - Milliliter	0703-4502	6e09e861-5b9d-4052-a6bd-5b708539b004	1	2024-10-04
0703-4502-94	ML - Milliliter	0703-4502	fdf9c277-d402-40d7-a220-a842ac3bfbad	1	2015-03-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
METOCLOPRAMIDE HYDROCHLORIDE	ACTIVE INGREDIENT	W1792A2RVD	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	8
METOCLOPRAMIDE	ACTIVE MOIETY	L4YEB44I46	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	8
HYDROCHLORIC ACID	INACTIVE INGREDIENT	QTT17582CB	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	8
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	8
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	8
WATER	INACTIVE INGREDIENT	059QF0KO0R	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	8
METOCLOPRAMIDE HYDROCHLORIDE	ACTIVE INGREDIENT	W1792A2RVD	METOCLOPRAMIDE HYDROCHLORIDE INJECTION [CARDINAL HEALTH]	3
METOCLOPRAMIDE	ACTIVE MOIETY	L4YEB44I46	METOCLOPRAMIDE HYDROCHLORIDE INJECTION [CARDINAL HEALTH]	3
hydrochloric acid	INACTIVE INGREDIENT	QTT17582CB	METOCLOPRAMIDE HYDROCHLORIDE INJECTION [CARDINAL HEALTH]	3
Sodium Chloride	INACTIVE INGREDIENT	451W47IQ8X	METOCLOPRAMIDE HYDROCHLORIDE INJECTION [CARDINAL HEALTH]	3
sodium hydroxide	INACTIVE INGREDIENT	55X04QC32I	METOCLOPRAMIDE HYDROCHLORIDE INJECTION [CARDINAL HEALTH]	3
Water	INACTIVE INGREDIENT	059QF0KO0R	METOCLOPRAMIDE HYDROCHLORIDE INJECTION [CARDINAL HEALTH]	3
METOCLOPRAMIDE HYDROCHLORIDE	ACTIVE INGREDIENT	W1792A2RVD	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
METOCLOPRAMIDE HYDROCHLORIDE	ACTIVE INGREDIENT	W1792A2RVD	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
METOCLOPRAMIDE	ACTIVE MOIETY	L4YEB44I46	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
METOCLOPRAMIDE	ACTIVE MOIETY	L4YEB44I46	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
HYDROCHLORIC ACID	INACTIVE INGREDIENT	QTT17582CB	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
HYDROCHLORIC ACID	INACTIVE INGREDIENT	QTT17582CB	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
SODIUM CHLORIDE	INACTIVE INGREDIENT	451W47IQ8X	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
SODIUM HYDROXIDE	INACTIVE INGREDIENT	55X04QC32I	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	METOCLOPRAMIDE INJECTION, SOLUTION [TEVA PARENTERAL MEDICINES, INC.]	1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 32 of 53 · 1,060 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
PhysiciansCare Ophthalmic Solution Eyewash	PURIFIED WATER 98.3%	Acme United Corporation	d3812fa3-9334-464d-b50c-98548ff76727	2024-11-26	Warnings	Exact identifier unii: 059QF0KO0R
DANGTTEOL	MINERAL WATER	AQBC CO., LTD	27db14a9-3812-433f-e063-6394a90a11e7	2024-11-26	Warnings	Exact identifier unii: 059QF0KO0R
ReHydration	ADENOSINUM CYCLOPHOSPHORICUM, COFFEA CRUDA, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS, KALI PHOS, NAT MUR, SARSAPARILLA, SILICEA, TARAXACUM, THYROIDINUM	Energetix Corporation	37063a49-6b45-4167-875d-49c9dac3f79b	2024-11-20	Warnings	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Baxter Healthcare Company	99a15716-bbb9-4e33-a48d-20c58b81f392	2024-11-13		Exact identifier unii: 451W47IQ8X
Metoclopramide	METOCLOPRAMIDE HYDROCHLORIDE	PAI Holdings, LLC dba PAI Pharma	3cc8ca5b-8b71-4c77-a181-9ce154597b9a	2024-11-13	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: W1792A2RVD
Itch Formula	ANTIPYRINUM, APIS MELLIFICA, CALENDULA OFFICINALIS, CANTHARIS, COPAIVA OFFICINALIS, CROTON TIGLIUM, GRAPHITES, HISTAMINUM HYDROCHLORICUM, LEDUM PALUSTRE, MEZEREUM, NATRUM MURIATICUM, PETROLEUM, RHUS VENENATA, STAPHYSAGRIA, SULPHUR, URTICA URENS	Deseret Biologicals, Inc.	4dfb177b-bff3-4b6d-8fd9-cadd1df7812c	2024-11-12	Warnings	Exact identifier unii: 451W47IQ8X
Plasma-Lyte 148 (pH 7.4)	SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE	Baxter Healthcare Corporation	fe935c8d-f42d-42e4-8665-0dc66829f231	2024-11-08		Exact identifier unii: 451W47IQ8X
Crane Safety Eye Wash	WATER SOLUTION	Crane Safety LLC	96d8dda9-6cd6-3f68-e053-2995a90a0da2	2024-11-08	Warnings	Exact identifier unii: 059QF0KO0R
RUGBY EYE WASH	WATER, PURIFIED	A-S Medication Solutions	0773e558-2f46-494c-888a-3bc517202b65	2024-11-08	Warnings	Exact identifier unii: 059QF0KO0R
Dextrose and Sodium Chloride	DEXTROSE MONOHYDRATE AND SODIUM CHLORIDE	BECTON DICKINSON AND COMPANY	d3f90d2f-4536-4d32-800b-7a798f8a35db	2024-11-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Hospira, Inc.	8eb172da-dcd4-4660-4a8f-ad44a14b4af7	2024-11-06	Adverse reactions	Exact identifier unii: 451W47IQ8X
Licefreee Everyday	SODIUM CHLORIDE	Tec Laboratories,Inc.	407b5fd6-2331-2ba7-e054-00144ff88e88	2024-11-05	Warnings	Exact identifier unii: 451W47IQ8X
Licefreee	HEAD LICE TREATMENT	Tec Laboratories, Inc.	08c9d3dd-7177-0148-e054-00144ff8d46c	2024-11-05	Warnings	Exact identifier unii: 451W47IQ8X
Bladder Relief	CAUSTICUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (VULGARIS), SEPIA, STAPHYSAGRIA, THUJA OCCIDENTALIS	Magni Company	5d0db70c-6360-493b-bcf2-8dbc95314140	2024-11-05	Warnings	Exact identifier unii: 451W47IQ8X
Vaccines	ARNICA MONTANA, HYPERICUM PERFORATUM, LEDUM PALUSTRE, MORBILLINUM, NATRUM MURIATICUM, SILICEA, SULPHUR IODATUM, THUJA OCCIDENTALIS, URTICA URENS	Liddell Laboratories, Inc.	6e6e67d4-089e-4775-b4a4-5511953f6e3f	2024-11-04	Warnings	Exact identifier unii: 451W47IQ8X
Gluten Detox	BARLEY (GRAIN), CARBO VEGETABILIS, CINCHONA OFFICINALIS, GLUTEN, GLYPHOSATE, HYDRASTIS CANADENSIS, LYCOPODIUM CLAVATUM, NATRUM MURIATICUM, NUX VOMICA, OAT (GRAIN), PANCREAS SUIS, PULSATILLA (VULGARIS), RYE (GRAIN), WHEAT (GRAIN)	Liddell Laboratories, Inc.	706f2e33-8674-4911-ba0a-4efc935e7739	2024-11-04	Warnings	Exact identifier unii: 451W47IQ8X
Derma Pain	CALENDULA OFFICINALIS, CROTON TIGLIUM, NATRUM MURIATICUM, PLANTAGO MAJOR, RHUS TOX, SARSAPARILLA (SMILAX REGELII)	Liddell Laboratories, Inc.	e02a5e99-aa27-4276-a785-7b5328d89fdc	2024-11-04	Warnings	Exact identifier unii: 451W47IQ8X
Vaccistat	BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, ALUMINA, ANTIMONIUM TARTARICUM, MEZEREUM, NATRUM MURIATICUM, MERCURIUS SOLUBILIS, SILICEA, THUJA OCCIDENTALIS, MALANDRINUM, VARIOLINUM	Energique, Inc.	8c8d63b6-763a-44f8-87ef-e83a89ec3776	2024-10-31	Warnings	Exact identifier unii: 451W47IQ8X
Vaccistat	BAPTISIA TINCTORIA, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, ALUMINA, ANTIMONIUM TARTARICUM, MEZEREUM, NATRUM MURIATICUM, MERCURIUS SOLUBILIS, SILICEA, THUJA OCCIDENTALIS, MALANDRINUM, VARIOLINUM	Energique, Inc.	5205cc3e-c9bc-48e9-9c9b-959a9be78b85	2024-10-31	Warnings	Exact identifier unii: 451W47IQ8X
Weed Grass Antigens	ALLIUM CEPA, ARSENICUM ALBUM, NATRUM MURIATICUM, NUX VOMICA, PULSATILLA (PRATENSIS), ABROTANUM (ARTEMISIA ABROTANUM), ABSINTHIUM, AGRIMONIA EUPATORIA, FLOS, ALFALFA, AMBROSIA ARTEMISIAEFOLIA, ARUNDO MAURITANICA, BAMBUSA ARUNDINACEA, CICHORIUM INTYBUS, FLOS, KENTUCKY BLUEGRASS, ORCHARD GRASS, BERMUDA GRASS, JOHNSON GRASS, RYE GRASS, VERNAL GRASS, BAHIA GRASS, TIMOTHY GRASS, RUMEX CRISPUS, SABADILLA, SINAPIS ARVENSIS, FLOS, SOLIDAGO VIRGAUREA, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE, TRIFOLIUM REPENS,	Energique, Inc.	0ec09d62-07ca-4bbe-9019-1025f5713211	2024-10-31	Warnings	Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.