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
TABLET
Routes
Active Ingredients
morphine sulfate 30 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0054-0236
Product ID
0054-0236_7d786bb9-4666-411d-bf62-24ae34f555d5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA022207
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2008-03-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00540236
Hyphenated Format
0054-0236
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
NDA022207 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (0054-0236-24) / 1 TABLET in 1 BLISTER PACK
- 100 TABLET in 1 BOTTLE (0054-0236-25)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7d786bb9-4666-411d-bf62-24ae34f555d5", "openfda": {"upc": ["0300540236250", "0300540235253"], "unii": ["X3P646A2J0"], "rxcui": ["892582", "892672"], "spl_set_id": ["3c847554-3b4b-4d24-a145-2ef7e9b83699"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0054-0236-24) / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0054-0236-24", "marketing_start_date": "20080317"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (0054-0236-25)", "package_ndc": "0054-0236-25", "marketing_start_date": "20080317"}], "brand_name": "Morphine Sulfate", "product_id": "0054-0236_7d786bb9-4666-411d-bf62-24ae34f555d5", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0054-0236", "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": "30 mg/1"}], "application_number": "NDA022207", "marketing_category": "NDA", "marketing_start_date": "20080317", "listing_expiration_date": "20261231"}