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 8 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76045-007
Product ID
76045-007_e064585d-2d2d-41cd-a0f1-43494ce4775b
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
76045007
Hyphenated Format
76045-007
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
- 8 mg/mL
Packaging
- 16 HOW SUPPLIED/STORAGE AND HANDLING Morphine Sulfate Injection is available for intravenous (IV) or intramuscular (IM) use as: Product Code Unit of Sale Strength Each 764412 NDC 76045-004-12 Unit of 24 2 mg/mL NDC 76045-004-02 1 mL single-dose prefilled syringe 764512 NDC 76045-005-12 Unit of 24 4 mg/mL NDC 76045-005-02 1 mL single-dose prefilled syringe 764612 NDC 76045-006-12 Unit of 24 5 mg/mL NDC 76045-006-02 1 mL single-dose prefilled syringe 764710 NDC 76045-007-10 Unit of 24 8 mg/mL NDC 76045-007-00 1 mL single-dose prefilled syringe 764810 NDC 76045-008-10 Unit of 24 10 mg/mL NDC 76045-008-00 1 mL single-dose prefilled syringe Store at 20°C to 25°C (68°F to 77°F) [See USP Controlled Room Temperature.] PROTECT FROM LIGHT. DO NOT FREEZE . This product is for single dose only.
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel Rx only NDC 76045-004-12 Morphine Sulfate Injection, USP CII 2 mg/mL For Intramuscular or Intravenous use. Do NOT place syringe on a Sterile Field. 24 X 1 mL single-dose prefilled syringes PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label Rx only NDC 76045-004-02 Morphine Sulfate Injection, USP CII 2 mg/mL For IM or IV use. 1 mL single-dose prefilled syringe PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Syringe Label For IM or IV use. 1 mL Single-Dose. Morphine Sulfate Injection, USP CII 2 mg/mL Rx only PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Syringe Label
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel Rx only NDC 76045-005-12 Morphine Sulfate Injection, USP CII 4 mg/mL For Intramuscular or Intravenous use. Do NOT place syringe on a Sterile Field. 24 X 1 mL single-dose prefilled syringes PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel
- PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Blister Pack Label Rx only NDC 76045-005-02 Morphine Sulfate Injection, USP CII 4 mg/mL For IM or IV use. 1 mL single-dose prefilled syringe PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Blister Pack Label
- PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label For IM or IV use. 1mL Single-Dose. Morphine Sulfate Injection, USP CII 4 mg/mL Rx only PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel Rx only NDC 76045-006-12 Morphine Sulfate Injection, USP CII 5 mg/mL For Intramuscular or Intravenous use. Do NOT place syringe on a Sterile Field. 24 X 1 mL single-dose prefilled syringes PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label Rx only NDC 76045-006-02 Morphine Sulfate Injection, USP CII 5 mg/mL For IM or IV use. 1 mL single-dose prefilled syringe PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label
- PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label For IM or IV use. 1 mL Single-Dose. Morphine Sulfate Injection, USP CII 5 mg/mL Rx only PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel Rx only NDC 76045-007-10 Morphine Sulfate Injection, USP CII 8 mg/mL For Intramuscular or Intravenous use. Do NOT place syringe on a Sterile Field. 24 X 1 mL single-dose prefilled syringes PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label Rx only NDC 76045-007-00 Morphine Sulfate Injection, USP CII 8 mg/mL For IM or IV use. 1 mL single-dose prefilled syringe PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label
- PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label For IM or IV use. 1 mL Single-Dose. Morphine Sulfate Injection, USP CII 8 mg/mL Rx only PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel Rx only NDC 76045-008-10 Morphine Sulfate Injection, USP CII 10 mg/mL For Intramuscular or Intravenous use. Do NOT place syringe on a Sterile Field. 24 X 1 mL single-dose prefilled syringes PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Carton Panel
- PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label Rx only NDC 76045-008-00 Morphine Sulfate Injection, USP CII 10 mg/mL For IM or IV use. 1 mL single-dose prefilled syringe PACKAGE LABEL - PRINCIPAL DISPLAY – Morphine 1 mL Blister Pack Label
- PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label For IM or IV use. 1 mL Single-Dose. Morphine Sulfate Injection, USP CII 10 mg/mL Rx only PACKAGE LABEL - PRINCIPAL DISPLAY - Morphine 1 mL Syringe Label
Packages (0)
No package records.
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "e064585d-2d2d-41cd-a0f1-43494ce4775b", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["894912", "894914", "998212", "998213", "1442790"], "spl_set_id": ["b62ee1ef-db55-417a-a02e-b103890f9c4b"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [], "brand_name": "Morphine Sulfate", "product_id": "76045-007_e064585d-2d2d-41cd-a0f1-43494ce4775b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76045-007", "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": "8 mg/mL"}], "application_number": "NDA204223", "marketing_category": "NDA", "marketing_start_date": "20131030", "listing_expiration_date": "20261231"}