morphine sulfate
Generic: morphine sulfate
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
morphine sulfate
Generic Name
morphine sulfate
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
morphine sulfate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-3815
Product ID
0409-3815_493a6182-2a85-4973-8a20-6bb2344d6452
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073510
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2005-06-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04093815
Hyphenated Format
0409-3815
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
ANDA073510 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 5 VIAL, GLASS in 1 CARTON (0409-3815-12) / 10 mL in 1 VIAL, GLASS (0409-3815-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INTRATHECAL", "INTRAVENOUS"], "spl_id": "493a6182-2a85-4973-8a20-6bb2344d6452", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["1728783", "1728800"], "spl_set_id": ["1d181906-f3ec-4222-1883-e61577a3122e"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL, GLASS in 1 CARTON (0409-3815-12) / 10 mL in 1 VIAL, GLASS (0409-3815-11)", "package_ndc": "0409-3815-12", "marketing_start_date": "20050629"}], "brand_name": "Morphine Sulfate", "product_id": "0409-3815_493a6182-2a85-4973-8a20-6bb2344d6452", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0409-3815", "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": "1 mg/mL"}], "application_number": "ANDA073510", "marketing_category": "ANDA", "marketing_start_date": "20050629", "listing_expiration_date": "20261231"}