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 40 of 53 · 1,060 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Fendall 2000 Pure Flow	PURIFIED WATER	Honeywell Safety Products USA, Inc.	b56ef662-fec2-4d94-e053-2995a90aba2b	2024-01-06	Warnings	Exact identifier unii: 059QF0KO0R
Sodium chloride	SODIUM CHLORIDE	Fresenius Kabi USA, LLC	037ac04d-f8f3-4bb8-993a-ac8f7683ff83	2024-01-04	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Leader Eye Wash	PURIFIED WATER	Cardinal Health	8d3ad11f-1945-f838-e053-2995a90a7aa5	2023-12-23	Warnings	Exact identifier unii: 059QF0KO0R
Sinus HP	ARSENICUM ALBUM, HEPAR SULPHURIS CALCAREUM, HYDRASTIS CANADENSIS, KALI BICHROMICUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, PHOSPHORUS, PULSATILLA (PRATENSIS), SEPIA, THUJA OCCIDENTALIS	Energique, Inc.	3cdddbe5-e3d2-4629-a045-868e18183f1d	2023-12-19	Warnings	Exact identifier unii: 451W47IQ8X
BSS	BALANCED SALT SOLUTION	Alcon Laboratories, Inc.	28488c7b-cf6a-4a03-916f-cc66b3afdc57	2023-12-14	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Altachlore Sodium Chloride Hypertonicity	SODIUM CHLORIDE	Altaire Pharmaceuticals Inc.	dc0d94d8-4475-4956-8ded-bdb9496074e4	2023-12-09	Warnings	Exact identifier unii: 451W47IQ8X
Eye Wash	WATER	Jiangxi Zhenmei Biological Technology Co.,Ltd	c68795b8-bf68-0d01-e053-2a95a90abebb	2023-12-04	Warnings	Exact identifier unii: 059QF0KO0R
terrasil Eczema and Psoriasis Severe Outbreak	GRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG	Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions	4d7128fb-57f1-4d0d-a83a-daef40928ecd	2023-11-30	Warnings	Exact identifier unii: 451W47IQ8X
terragen HG Formula Maximum Strength	GRAPHITE, SODIUM CHLORIDE, SYMPHYTUM OFFICINALE WHOLE, THUJA OCCIDENTALIS LEAFY TWIG	Aidance Scientific, Inc, DBA Aidance Skincare & Topical Solutions	e632c831-e25d-4d04-ba72-2327d25713b1	2023-11-30	Warnings	Exact identifier unii: 451W47IQ8X
Femstat C	ECHINACEA (ANGUSTIFOLIA), FUCUS VESICULOSUS, HYDRASTIS CANADENSIS, PHYTOLACCA DECANDRA, KREOSOTUM, NATRUM MURIATICUM, CANDIDA ALBICANS, LYCOPODIUM CLAVATUM, PULSATILLA (PRATENSIS), SEPIA	Energique, Inc.	420119ca-f2bf-40e3-9e40-00498724c228	2023-11-30	Warnings	Exact identifier unii: 451W47IQ8X
Endopar	GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, HYPOTHALAMUS SUIS, OOPHORINUM (SUIS), ORCHITINUM (BOVINE), PINEAL GLAND, THYROIDINUM, ARSENICUM ALBUM, BARYTA CARBONICA, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PULSATILLA (PRATENSIS)	Energique, Inc.	06375c3e-cc05-4450-9117-1d3dc72636eb	2023-11-21	Warnings	Exact identifier unii: 451W47IQ8X
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	8643994f-4e13-4572-e053-2991aa0a5b78	2023-11-14		Exact identifier unii: QTT17582CB
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	6907bbfe-caa5-2ce4-e053-2991aa0ade8d	2023-11-14		Exact identifier unii: QTT17582CB
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	8643c518-13b2-658a-e053-2a91aa0ac5ed	2023-11-14		Exact identifier unii: QTT17582CB
Muriaticum acidum	HYDROCHLORIC ACID	Boiron	8643e30e-1f47-09f1-e053-2991aa0ac2de	2023-11-14		Exact identifier unii: QTT17582CB
Natrum muriaticum	SODIUM CHLORIDE	Boiron	8646d7ea-cf5e-607d-e053-2a91aa0aeca1	2023-11-14		Exact identifier unii: 451W47IQ8X
Natrum muriaticum	SODIUM CHLORIDE	Boiron	86466121-7217-d053-e053-2a91aa0a8f8a	2023-11-14		Exact identifier unii: 451W47IQ8X
Natrum muriaticum	SODIUM CHLORIDE	Boiron	864669c9-5bdc-232f-e053-2a91aa0a1fc6	2023-11-14		Exact identifier unii: 451W47IQ8X
Natrum muriaticum	SODIUM CHLORIDE	Boiron	86462e06-d221-36b7-e053-2991aa0a1d82	2023-11-14		Exact identifier unii: 451W47IQ8X
CV TOX	COCHLEARIA ARMORACIA, ECHINACEA (ANGUSTIFOLIA), LOMATIUM DISSECTUM, TABEBUIA IMPETIGINOSA, HYDRASTIS CANADENSIS, PROPOLIS, GLANDULA SUPRARENALIS BOVINE, THYMUS (SUIS), ARANEA DIADEMA, IPECACUANHA, LYCOPODIUM CLAVATUM, MURIATICUM ACIDUM, NITRICUM ACIDUM, PHOSPHORICUM ACIDUM, RHUS TOX, SILICEA, EPSTEIN-BARR VIRUS NOSODE, HERPES ZOSTER NOSODE, MORBILLINUM, POLIOMYELITIS NOSODE, HEPATITIS B NOSODE, COXSACKIE B1 NOSODE, CYTOMEGALOVIRUS NOSODE, COXSACKIE B4 NOSODE, EPSTEIN BARR VIRUS NOSODE	BioActive Nutritional, Inc.	8ef2fb5c-1b24-46a1-8d21-a78ce0a34a87	2023-11-07	Warnings	Exact identifier unii: QTT17582CB

Reported adverse events (FAERS/openFDA)#

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