morphine sulfate
Generic: morphine sulfate
Labeler: sun pharmaceutical industries, inc.Drug Facts
Product Profile
Brand Name
morphine sulfate
Generic Name
morphine sulfate
Labeler
sun pharmaceutical industries, inc.
Dosage Form
TABLET, FILM COATED, EXTENDED RELEASE
Routes
Active Ingredients
morphine sulfate 60 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63304-758
Product ID
63304-758_39a0166a-c2ca-47bf-8654-85e0a431b9a0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078761
DEA Schedule
cii
Listing Expiration
2026-12-31
Marketing Start
2012-05-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63304758
Hyphenated Format
63304-758
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
ANDA078761 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 60 mg/1
Packaging
- 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-01)
- 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-03)
- 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-05)
- 50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-50)
Packages (4)
63304-758-01
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-01)
63304-758-03
10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-03)
63304-758-05
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-05)
63304-758-50
50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-50)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "39a0166a-c2ca-47bf-8654-85e0a431b9a0", "openfda": {"upc": ["0363304453010", "0363304758016", "0363304452013", "0363304450019", "0363304451016"], "unii": ["X3P646A2J0"], "rxcui": ["891874", "891881", "891888", "891893", "892646"], "spl_set_id": ["736c9b80-682c-4cda-bf18-61b18de0bd39"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-01)", "package_ndc": "63304-758-01", "marketing_start_date": "20120511"}, {"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-03)", "package_ndc": "63304-758-03", "marketing_start_date": "20120511"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-05)", "package_ndc": "63304-758-05", "marketing_start_date": "20120511"}, {"sample": false, "description": "50 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-758-50)", "package_ndc": "63304-758-50", "marketing_start_date": "20120511"}], "brand_name": "Morphine sulfate", "product_id": "63304-758_39a0166a-c2ca-47bf-8654-85e0a431b9a0", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63304-758", "dea_schedule": "CII", "generic_name": "morphine sulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "60 mg/1"}], "application_number": "ANDA078761", "marketing_category": "ANDA", "marketing_start_date": "20120511", "listing_expiration_date": "20261231"}