morphine sulfate
Generic: morphine sulfate
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
morphine sulfate
Generic Name
morphine sulfate
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION
Routes
Active Ingredients
morphine sulfate 4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0641-6125
Product ID
0641-6125_fa18221d-2353-4cf6-a210-fb33ee79d3d9
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA205758
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2015-06-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
06416125
Hyphenated Format
0641-6125
Supplemental Identifiers
RxCUI
UPC
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
ANDA205758 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 PACKAGE (0641-6125-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0641-6125-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fa18221d-2353-4cf6-a210-fb33ee79d3d9", "openfda": {"upc": ["0306416126250", "0306416127257", "0306416125253"], "unii": ["X3P646A2J0"], "rxcui": ["1731993", "1732006", "1732011"], "spl_set_id": ["6023606c-150c-40c5-9175-598efe2a56c3"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 PACKAGE (0641-6125-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0641-6125-01)", "package_ndc": "0641-6125-25", "marketing_start_date": "20150603"}], "brand_name": "Morphine Sulfate", "product_id": "0641-6125_fa18221d-2353-4cf6-a210-fb33ee79d3d9", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6125", "dea_schedule": "CII", "generic_name": "Morphine Sulfate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine Sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "4 mg/mL"}], "application_number": "ANDA205758", "marketing_category": "ANDA", "marketing_start_date": "20150603", "listing_expiration_date": "20261231"}