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 47 of 60 · 1,198 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Natrum muriaticum	SODIUM CHLORIDE	Boiron	86462e06-d221-36b7-e053-2991aa0a1d82	2023-11-14		Exact identifier unii: 451W47IQ8X
Mineffect nasal mist	CALCAREA SILICATA, SILICEA, SULPHUR, NATRUM MURIATICUM, FERRUM METALLICUM, FERRUM PHOSPHORICUM, PHOSPHORUS, FERRUM MURIATICUM, TITANIUM METALLICUM,	Kadesh Incoporation Co,Ltd	3a29bf95-a8a3-4517-aedf-0cd4a91b349c	2023-10-31	Warnings	Exact identifier unii: 451W47IQ8X
Insomnia	AQUILEGIA VULGARIS, AVENA SATIVA, CHAMOMILLA, COFFEA CRUDA, CYPRIPEDIUM PUBESCENS, HUMULUS LUPULUS, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, MELATONIN, MELISSA OFFICINALIS, NATRUM MURIATICUM, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS	Liddell Laboratories, Inc.	18c15f17-1a16-4595-9d23-20353363cd72	2023-10-31	Warnings	Exact identifier unii: 451W47IQ8X
Saline	NASAL	GERI-CARE PHARMACEUTICAL CORP	d293cc13-4043-0d58-e053-2995a90a3fbc	2023-10-24	Warnings	Exact identifier unii: 451W47IQ8X
Natrum muriaticum	SODIUM CHLORIDE	Boiron	8644ffef-f0ec-5c06-e053-2a91aa0ae83d	2023-10-23		Exact identifier unii: 451W47IQ8X
Aqua marina	SODIUM CHLORIDE	Boiron	6a212a52-32be-21b8-e053-2991aa0aea2f	2023-10-22		Exact identifier unii: 451W47IQ8X
Metab	CALCAREA SULPHURICA, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, CEREBELLUM (SUIS), GALLBLADDER (BOVINE), HEART (BOVINE), HEPAR (BOVINE), HYPOTHALAMUS SUIS, INTESTINE (SUIS), KIDNEY (BOVINE), LUNG (BOVINE), MEDULLA OSSIS SUIS, PANCREAS SUIS, PINEAL GLAND (SUIS), RECTAL MUCOSA (SUIS), SPLEEN (BOVINE), STOMACH (SUIS), THYMUS (OVINE), THYROIDINUM (BOVINE), URINARY BLADDER (SUIS), PITUITARUM POSTERIUM (BOVINE), ACETYL COENZYME A,	Nutritional Specialties, Inc.	bbed9973-238f-47c5-9a50-ac0869a7eb3a	2023-10-09	Warnings	Exact identifier unii: 451W47IQ8X
Isolyte S pH 7.4	SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, MAGNESIUM CHLORIDE, SODIUM PHOSPHATE, DIBASIC, AND POTASSIUM PHOSPHATE	B. Braun Medical Inc.	150437b6-320e-4c69-a434-2a26a1f0b2e4	2023-10-06	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Physiolyte	SODIUM CHLORIDE, SODIUM GLUCONATE, SODIUM ACETATE, POTASSIUM CHLORIDE, AND MAGNESIUM CHLORIDE	B. Braun Medical Inc.	19c04dcb-d6f2-4624-afd4-1c7b7ddcb85e	2023-09-26	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X
Allergies	APIS MELLIFICA, ECHINACEA, HYDRASTIS CANADENSIS, TARAXACUM OFFICINALE, ACONITUM NAPELLUS, AETHUSA CYNAPIUM, AGARICUS MUSCARIUS, ALETRIS FARINOSA, ALFALFA, ALLIUM CEPA, ALLIUM SATIVUM, AMBROSIA ARTEMISIAEFOLIA, ARSENICUM ALBUM, ARTEMISIA VULGARIS, ARUNDO MAURITANICA, AVENA SATIVA, BELLADONNA, BELLIS PERRENIS, BOVISTA, BROMIUM, BRYONIA, CAFFEINUM, CALCAREA CARBONICA, CALLUNA VULGARIS, FLOS, CAPSICUM ANNUUM, CAT HAIR, CHAMOMILLA, CHELIDONIUM MAJUS, CHENOPODIUM ANTHELMINTICUM, CINNAMOMUM	Newton Laboratories, Inc.	0631d5e5-9da4-bcb7-e063-6394a90a62de	2023-09-25	Warnings	Exact identifier unii: 451W47IQ8X
Epiforce P-HP	ARSENICUM ALBUM, BORAX, GRAPHITES, NATRUM MURIATICUM, SEPIA, SULPHUR	BioActive Nutritional, Inc.	250441d1-e261-417e-9100-700368ea38fd	2023-09-11	Warnings	Exact identifier unii: 451W47IQ8X
Lactated Ringers	SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, AND CALCIUM CHLORIDE	B. Braun Medical Inc.	a9910e09-5aea-4ee1-a35e-ae4abf8b80b4	2023-09-07	Warnings, Adverse reactions	Exact identifier unii: 451W47IQ8X unii: M4I0D6VV5M
ANUBISMED	HA HYALURONIC	ANUBIS COSMETICS SL	eac771e2-4c1b-3808-e053-2995a90ac5fc	2023-09-05	Warnings	Exact identifier unii: 059QF0KO0R
AnubisMed	SPF 50 BROAD SPECTRUM PROTECTION FLUID EMULSION	ANUBIS COSMETICS SL	e99d92c4-8768-9c0a-e053-2a95a90a609e	2023-09-05	Warnings	Exact identifier unii: 059QF0KO0R
AnubisMed	AZELAIC ACID, SALICYLIC ACID	ANUBIS COSMETICS SL	ebf3153d-30f5-54e4-e053-2995a90a74b1	2023-09-05	Warnings	Exact identifier unii: 059QF0KO0R
AnubisMed	GLYCOLIC ACID, CITRIC ACID, LACTIC ACID, KOJIC ACID	ANUBIS COSMETICS SL	eca95dde-cb57-2ab6-e053-2995a90af84f	2023-09-05	Warnings	Exact identifier unii: 059QF0KO0R
AnubisMed	SODIUM BICARBONATE, ALOE BARBADENSIS LEAF JUICE, IMIDAZOLIDINYL UREA	ANUBIS COSMETICS SL	ebf4b3ab-34e1-185a-e053-2a95a90ace3a	2023-09-05	Warnings	Exact identifier unii: 059QF0KO0R
Anubis Barcelona	GLYCERIN, SORBITOL, ALOE BARBADENSIS LEAF JUICE	ANUBIS COSMETICS SL	eb651769-4d98-2b3b-e053-2a95a90a36b0	2023-09-01	Warnings	Exact identifier unii: 059QF0KO0R
Anubis Barcelona	DMAE	ANUBIS COSMETICS SL	f22b212d-d21d-5984-e053-2995a90a683e	2023-09-01	Warnings	Exact identifier unii: 059QF0KO0R
Anubis Barcelona	DMAE, ZIRHAFIRM	ANUBIS COSMETICS SL	f2274f8c-08aa-eb02-e053-2a95a90a3998	2023-09-01	Warnings	Exact identifier unii: 059QF0KO0R

Reported adverse events (FAERS/openFDA)#

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