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 47 of 53 · 1,060 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Eye wash	PURIFIED WATER	McKesson	bd089fde-24ba-4de5-e053-2995a90a39bb	2022-10-18	Warnings	Exact identifier unii: 059QF0KO0R
Bach Original Flower Remedies Rock Water	WATER	Nelson Bach USA Limited	ea242559-1618-3354-e053-2a95a90a1a95	2022-10-03	Warnings	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Medical Purchasing Solutions, LLC	e90b47e3-9636-b9ee-e053-2a95a90ad48c	2022-09-19	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Dr Talbots Infant Daily Allergy Relief	ALLIUM CEPA 12X,ARALIA RACEMOSA 12X,EUPHRASIA OFFICINALIS 12X,GALPHIMIA GLAUCA 12X,HISTAMINUM HYDROCHLORICUM 12X,LUFFA OPERCULATA 12X,PULSATILLA 12X,SOLIDAGO 12X,NATRUM MURIATICUM 6X	Talbot's Pharmaceuticals Family Products,LLC.	e8bdcc8a-c947-ff5d-e053-2a95a90a3b92	2022-09-12	Warnings	Exact identifier unii: 451W47IQ8X
Herplex	ANATHERUM MURICATUM, CLEMATIS ERECTA, MEZEREUM, PHYTOLACCA DECANDRA, RANUNCULUS BULBOSUS, RHUS TOX, THUJA OCCIDENTALIS, NATRUM MURIATICUM, SEPIA	Nashco Products LLC	6a1322c7-7767-4569-aa22-9d2e36331283	2022-08-30	Warnings	Exact identifier unii: 451W47IQ8X
Kids Cold and Cough Nighttime Grape Flavor	ONION, CHAMOMILE, ARABICA COFFEE BEAN, CALCIUM SULFIDE, GOLDEN SEAL, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS TOP, SULFUR	Hyland's Consumer Health Inc.	e676dbb7-212f-47e3-e053-2995a90af4e1	2022-08-17	Warnings	Exact identifier unii: 451W47IQ8X
Kids Cold and Cough Daytime Grape Flavor	ONION, CALCIUM SULFIDE, GOLDEN SEAL, SODIUM CHLORIDE, PHOSPHORUS, PULSATILLA VULGARIS WHOLE, SULFUR	Hyland's Consumer Health Inc.	e65f14cb-5a8e-0ad5-e053-2a95a90a6f5d	2022-08-16	Warnings	Exact identifier unii: 451W47IQ8X
Sterile Saline Kids Mist PediaMeds	SODIUM CHLORIDE	ASCENT CONSUMER PRODUCTS, INC.	e5c5b580-1d9f-3081-e053-2995a90a8031	2022-08-08	Warnings	Exact identifier unii: 451W47IQ8X
Sterile Saline Kids Mist SinuCleanse Breathe	SODIUM CHLORIDE	ASCENT CONSUMER PRODUCTS, INC.	e5c5c313-046f-b0a7-e053-2a95a90a2a07	2022-08-08	Warnings	Exact identifier unii: 451W47IQ8X
SODIUM CHLORIDE	SODIUM CHLORIDE	Baxter Healthcare Corporation	123bd10a-90c7-499e-97f6-acf7e0f0fb4e	2022-07-29	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Herplex	ANATHERUM MURICATUM, CLEMATIS ERECTA, MEZEREUM, PHYTOLACCA DECANDRA, RANUNCULUS BULBOSUS, RHUS TOX, THUJA OCCIDENTALIS, NATRUM MURIATICUM, SEPIA	Nashco Products LLC	fad9615f-7004-415d-9f69-ee9ff95f0067	2022-07-12	Warnings	Exact identifier unii: 451W47IQ8X
BHI Constipation	DIOSCOREA VILLOSA TUBER, SODIUM CHLORIDE, AND STRYCHNOS NUX-VOMICA SEED	MediNatura Inc	0365b75b-fee4-4c1d-89ab-c692bdd73f75	2022-07-07	Warnings	Exact identifier unii: 451W47IQ8X
Natrium Muriaticum 6X	SODIUM CHLORIDE	Seroyal USA	0ebf18de-12fe-0bc4-e054-00144ff88e88	2022-07-07	Warnings	Exact identifier unii: 451W47IQ8X
Erogetone	ARALIA QUINQUEFOLIA, BERBERIS VULGARIS, CAUSTICUM, CONIUM MACULATUM, DAMIANA, GRAPHITES, LACHESIS MUTUS, NATRUM MURIATICUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, SEPIA	Energique, Inc.	1e872ecd-e7a5-463d-9832-47b7046096db	2022-06-28	Warnings	Exact identifier unii: 451W47IQ8X
Sterile Water	WATER	Fresenius Kabi USA, LLC	f42ac50f-0ec5-4713-a4c8-99d972d90bed	2022-06-22	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Sterile Water	WATER	Fresenius Kabi USA, LLC	e71c6c83-d518-496c-b2ab-efd5987e4783	2022-06-09	Warnings, Adverse reactions	Exact identifier unii: 059QF0KO0R
Cardioplegic Solution	POTASSIUM CHLORIDE, SODIUM CHLORIDE, CALCIUM CHLORIDE, AND MAGNESIUM CHLORIDE	Fresenius Kabi, USA, LLC	eb360dc4-88d6-4b28-9b61-bc359e16bd22	2022-05-27	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	24a08a93-df23-474b-873e-c59ec8855f9f	2022-03-14	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Wild Horse 777 Moisturizing Nasal	SODIUM CHLORIDE	Wild Horse 777, Inc.	b0b4dadd-11fa-3dbb-e053-2995a90a2097	2022-03-14	Warnings	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	B. Braun Medical Inc.	cc14fafd-3dcd-4fc8-bdbd-6f355c375768	2022-02-23	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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