morphine sulfate
Generic: morphine sulfate
Labeler: fresenius kabi, usa llcDrug Facts
Product Profile
Brand Name
morphine sulfate
Generic Name
morphine sulfate
Labeler
fresenius kabi, usa llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
morphine sulfate 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76045-004
Product ID
76045-004_286bce70-23cd-4d5b-989b-230d6cdd5a91
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA204223
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2013-10-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76045004
Hyphenated Format
76045-004
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
morphine sulfate (source: ndc)
Generic Name
morphine sulfate (source: ndc)
Application Number
NDA204223 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 10 SYRINGE, GLASS in 1 CARTON (76045-004-11) / 1 mL in 1 SYRINGE, GLASS (76045-004-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "286bce70-23cd-4d5b-989b-230d6cdd5a91", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["894912", "894914", "998212", "998213", "1442790"], "spl_set_id": ["1f53de80-efc8-4930-b3e3-fba0d026af05"], "manufacturer_name": ["Fresenius Kabi, USA LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 SYRINGE, GLASS in 1 CARTON (76045-004-11) / 1 mL in 1 SYRINGE, GLASS (76045-004-01)", "package_ndc": "76045-004-11", "marketing_start_date": "20191125"}], "brand_name": "Morphine Sulfate", "product_id": "76045-004_286bce70-23cd-4d5b-989b-230d6cdd5a91", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76045-004", "dea_schedule": "CII", "generic_name": "Morphine Sulfate", "labeler_name": "Fresenius Kabi, USA LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine Sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "2 mg/mL"}], "application_number": "NDA204223", "marketing_category": "NDA", "marketing_start_date": "20131030", "listing_expiration_date": "20261231"}