morphine sulfate

Generic: morphine sulfate

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name morphine sulfate
Generic Name morphine sulfate
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

morphine sulfate 50 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-1134
Product ID 0409-1134_a641ae70-f6ba-4f49-b5fc-b2895ef3408f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2005-08-11

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04091134
Hyphenated Format 0409-1134

Supplemental Identifiers

RxCUI
1731517 1731537 1731545
UNII
X3P646A2J0

Packaging Origin

Original Packager
true

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)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1134-03) / 20 mL in 1 VIAL, SINGLE-DOSE
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1134-05) / 50 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (2)

Ingredients (1)

morphine sulfate (50 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "a641ae70-f6ba-4f49-b5fc-b2895ef3408f", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["1731517", "1731537", "1731545"], "spl_set_id": ["cadc3fdb-8edc-44cd-aaea-89e68aaf9a04"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1134-03)  / 20 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-1134-03", "marketing_start_date": "20050927"}, {"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0409-1134-05)  / 50 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0409-1134-05", "marketing_start_date": "20050811"}], "brand_name": "Morphine Sulfate", "product_id": "0409-1134_a641ae70-f6ba-4f49-b5fc-b2895ef3408f", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0409-1134", "dea_schedule": "CII", "generic_name": "MORPHINE SULFATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine Sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "50 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20050811", "listing_expiration_date": "20261231"}