NDC 76045-005-01 - Morphine Sulfate

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: 76045-005
Requested NDC: 76045-005-01
Package NDCs from labels: 76045-005-01, 76045-005-11, 76045-005-02, 76045-005-12
Manufacturer: Fresenius Kabi, USA LLC | Fresenius Kabi USA, LLC
Effective date: 2026-08-31
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Morphine Sulfate - Fresenius Kabi, USA LLC \| Fresenius Kabi USA, LLC	Fresenius Kabi, USA LLC \| Fresenius Kabi USA, LLC	2026-08-31	HUMAN PRESCRIPTION DRUG LABEL
Morphine Sulfate - Fresenius Kabi USA, LLC	Fresenius Kabi USA, LLC	2025-09-04	HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
76045-005-01	Morphine Sulfate	1 mL in 1 SYRINGE, GLASS	INJECTION, SOLUTION	1		7
76045-005-11	Morphine Sulfate	10 in 1 CARTON	INJECTION, SOLUTION	10		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
76045-005	MORPHINE SULFATE (MORPHINE SULFATE) INJECTION, SOLUTION [FRESENIUS KABI USA, LLC ]	17	Current NDC, Legacy NDC	20210310_b62ee1ef-db55-417a-a02e-b103890f9c4b.zip
76045-005	MORPHINE SULFATE INJECTION, SOLUTION [FRESENIUS KABI, USA LLC]	7	Current NDC, Legacy NDC, 2 package rows	20250412_1f53de80-efc8-4930-b3e3-fba0d026af05.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
76045-005-01	ML - Milliliter	76045-005	5c978217-da01-4faa-967c-2d8bbc49ae42	1	2020-05-08
76045-005-10	ML - Milliliter	76045-005	9e55d236-0483-42b1-a9cd-9133d4ab23bd	1	2014-05-02
76045-005-11	ML - Milliliter	76045-005	60795206-cf27-4003-b569-ce714cb0a73a	1	2020-05-08

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
Morphine Sulfate	ACTIVE INGREDIENT	X3P646A2J0	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5
Morphine	ACTIVE MOIETY	76I7G6D29C	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5
Calcium Chloride	INACTIVE INGREDIENT	M4I0D6VV5M	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5
Citric Acid Monohydrate	INACTIVE INGREDIENT	2968PHW8QP	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5
Edetate Disodium	INACTIVE INGREDIENT	7FLD91C86K	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5
Sodium chloride	INACTIVE INGREDIENT	451W47IQ8X	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5
Trisodium Citrate Dihydrate	INACTIVE INGREDIENT	B22547B95K	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5
Water	INACTIVE INGREDIENT	059QF0KO0R	MORPHINE SULFATE INJECTION, SOLUTION [BD RX INC.]	5

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 36 of 60 · 1,198 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Morphine Sulfate Extended Release	MORPHINE SULFATE	American Health Packaging	f915420d-981d-455b-b4cf-67c8e201a136	2024-12-30	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: X3P646A2J0
Morphine Sulfate	MORPHINE SULFATE	International Medication Systems, Limited	1034467f-d436-4b87-a902-c7e8885daa8a	2024-12-30	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: X3P646A2J0
Gut Brain Spectrum	ABROTANUM (ARTEMISIA ABROTANUM), AETHUSA CYNAPIUM, BAPTISIA TINCTORIA, CICUTA VIROSA, CUPRUM METALLICUM, MEZEREUM, BUFO RANA, LAC MATERNA HUMANUM, SACCHARUM OFFICINALE, SEROTONIN (HYDROCHLORIDE), ALUMINA, CALCAREA PHOSPHORICA, CANDIDA ALBICANS, CARCINOSIN, LAC CANINUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, PROPIONIC ACID, SULPHUR, THUJA OCCIDENTALIS, FORMALINUM, MORBILLINUM	Energique, Inc.	adfee6ce-05b0-4955-bf5f-9612b8db4c78	2024-12-26	Warnings	Exact identifier unii: 451W47IQ8X
TREE ANTIGEN	POPULUS TRISTIS POLLEN, JUGLANS NIGRA POLLEN, ACER NEGUNDO POLLEN, ALNUS RUBRA POLLEN, JUNIPERUS VIRGINIANA POLLEN, ULMUS RUBRA POLLEN, ACER PSEUDOPLANUS POLLEN, FRAXINUS AMERICANA POLLEN, CARYA TOMENTOSA POLLEN, ONION, ARSENIC TRIOXIDE, ATROPA BELLADONNA, ACTIVATED CHARCOAL, EUPHRASIA OFFICINALIS, LYCOPODIUM CLAVITUM SPORE, SODIUM CHLORIDE, STRYCHNOS NUX-VOMICA SEED, PULSITILLA VULGARIS WHOLE	Natural Creations, Inc	8040ab36-90eb-4076-a478-9b82ccfa4ec9	2024-12-23	Warnings	Exact identifier unii: 451W47IQ8X
Sterile Hypertonic Saline Solution 7 Sodium Chloride	SODIUM CHLORIDE	JOONEM LLC	e7110525-9f9b-5b68-e053-2995a90ac034	2024-12-23	Warnings	Exact identifier unii: 451W47IQ8X
Base Laboratories Saline	SODIUM CHLORIDE	Joonem LLC	49309411-9af4-4f19-a3bf-dbeabc106827	2024-12-23	Warnings	Exact identifier unii: 451W47IQ8X
Base Laboratories Saline	SODIUM CHLORIDE	Joonem LLC	ba0868f6-d3de-40e2-bcb3-144fa53062c7	2024-12-23	Warnings	Exact identifier unii: 451W47IQ8X
Base Laboratories Saline	SODIUM CHLORIDE	Joonem LLC	9d83f477-ebbc-4248-8445-769178181d4f	2024-12-23	Warnings	Exact identifier unii: 451W47IQ8X
Calcium Chloride	CALCIUM CHLORIDE	Dr. Reddy's Laboratories Inc.	7e94daf8-b71f-49d9-af3f-3a78ae9dfc8a	2024-12-19	Warnings, Adverse reactions	Exact identifier unii: M4I0D6VV5M
Trace Mineral Cord	ARGENTUM METALLICUM, AURUM METALLICUM, BORON CITRATE, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, CHROMIUM SULPHURICUM, COBALT GLUCONATE, CUPRUM SULPHURICUM, FERRUM PHOSPHORICUM, GERMANIUM SESQUIOXIDE, IODIUM, KALI BROMATUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, MANGANUM MURIATICUM, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SELENIUM METALLICUM, SILICEA, SODIUM MOLYBDATE, STRONTIUM CARBONICUM, VANADIUM METALLICUM,	Energique, Inc.	902dd68d-5ce1-481e-8938-6487dcc68dfc	2024-12-19	Warnings	Exact identifier unii: 451W47IQ8X
Calcium Chloride Dihydrate	CALCIUM CHLORIDE DIHYDRATE	Somerset Therapeutics, LLC	8f22eef7-cb4b-41c9-9fe4-7010aadf2164	2024-12-19	Warnings, Adverse reactions	Exact identifier unii: M4I0D6VV5M
Ancient Secrets Breathe Again	SODIUM CHLORIDE	LOTUS BRANDS, INC.	c6d2bab0-d363-4c09-a71b-ae15db915b37	2024-12-18	Warnings	Exact identifier unii: 451W47IQ8X
Walgreens Saline Mist Extra Strength	SODIUM CHLORIDE	Walgreen's Corporation	90cbe2dc-36b6-77fb-e053-2995a90a2897	2024-12-18	Warnings	Exact identifier unii: 451W47IQ8X
CVS Health Sterile Saline Mist	SODIUM CHLORIDE	CVS Pharmacy	6f1fe980-ca09-401d-aed6-d3d3387cc49a	2024-12-18	Warnings	Exact identifier unii: 451W47IQ8X
Mast Cell Pro	HYDRASTIS CANADENSIS, ASCORBICUM ACIDUM, CINCHONA OFFICINALIS, KIDNEY (SUIS), THIAMINUM HYDROCHLORICUM, URTICA DIOICA, APIS MELLIFICA, ARSENICUM ALBUM, BOVISTA, CARBOLICUM ACIDUM, COFFEA CRUDA, HISTAMINUM HYDROCHLORICUM, LACHESIS MUTUS, LEDUM PALUSTRE, NUX VOMICA, OXALICUM ACIDUM, PHOSPHORUS, RHUS TOX, SARCOLACTICUM ACIDUM, SECALE CORNUTUM, SEPIA, SEROTONIN (HYDROCHLORIDE), SULPHUR, THUJA OCCIDENTALIS, VENUS MERCENARIA, ACONITUM NAPELLUS, CALADIUM SEGUINUM, IGNATIA AMARA, NATRUM MURIATICUM,	Energique, Inc.	5cd31e1d-0312-48d1-9ecd-d01c6fe3b672	2024-12-11	Warnings	Exact identifier unii: 451W47IQ8X
Fendall Pure Flow	PURIFIED WATER	Honeywell Safety Products USA, Inc.	afda6fc3-7615-b0be-e053-2995a90a6208	2024-12-10	Warnings	Exact identifier unii: 059QF0KO0R
Morphine Sulfate	MORPHINE SULFATE	Bryant Ranch Prepack	9bb1fef7-4159-4dca-8a8c-37e53ccc6bab	2024-12-06	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: X3P646A2J0
Junior Moves	ANACARDIUM, BRYONIA, MAG MUR, NAT MUR, PLUMB MET	Silver Star Brands	822d5481-7854-3fe7-e053-2a91aa0abf55	2024-12-03	Warnings	Exact identifier unii: 451W47IQ8X
Migo-Ease	ACONITUM NAP, LYCOPODIUM, NAT MUR, NUX VOM, PULSATILLA	Silver Star Brands	816837f5-4487-657d-e053-2991aa0a78f4	2024-12-03	Warnings	Exact identifier unii: 451W47IQ8X
Sodium Chloride	SODIUM CHLORIDE	Baxter Healthcare Company	464c2d78-5c88-4668-a039-56dd3c1c9b20	2024-12-03		Exact identifier unii: 451W47IQ8X

Reported adverse events (FAERS/openFDA)#

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