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 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76045-008
Product ID
76045-008_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
76045008
Hyphenated Format
76045-008
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
- 10 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": "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": [], "brand_name": "Morphine Sulfate", "product_id": "76045-008_286bce70-23cd-4d5b-989b-230d6cdd5a91", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "76045-008", "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": "10 mg/mL"}], "application_number": "NDA204223", "marketing_category": "NDA", "marketing_start_date": "20131030", "listing_expiration_date": "20261231"}