morphine sulfate

Generic: morphine sulfate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morphine sulfate
Generic Name morphine sulfate
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

morphine sulfate 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1791
Product ID 72162-1791_0c6a93c2-80bb-47dc-9a64-717724b23302
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078761
DEA Schedule cii
Marketing Start 2012-05-11
Marketing End 2026-12-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621791
Hyphenated Format 72162-1791

Supplemental Identifiers

RxCUI
891874
UNII
X3P646A2J0

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-1)
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-3)
  • 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-6)
  • 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-9)
source: ndc

Packages (4)

72162-1791-1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-1) 72162-1791-3 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-3) 72162-1791-6 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-6) 72162-1791-9 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-9)

Ingredients (1)

morphine sulfate (100 mg/1)

Linked Drug Pages (1)

Morphine sulfate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "0c6a93c2-80bb-47dc-9a64-717724b23302", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["891874"], "spl_set_id": ["3a89d0ca-4ff8-4bdc-8ea8-9ad591ce7226"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-1)", "package_ndc": "72162-1791-1", "marketing_end_date": "20261231", "marketing_start_date": "20120511"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-3)", "package_ndc": "72162-1791-3", "marketing_end_date": "20261231", "marketing_start_date": "20120511"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-6)", "package_ndc": "72162-1791-6", "marketing_end_date": "20261231", "marketing_start_date": "20120511"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1791-9)", "package_ndc": "72162-1791-9", "marketing_end_date": "20261231", "marketing_start_date": "20120511"}], "brand_name": "Morphine sulfate", "product_id": "72162-1791_0c6a93c2-80bb-47dc-9a64-717724b23302", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1791", "dea_schedule": "CII", "generic_name": "morphine sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "100 mg/1"}], "application_number": "ANDA078761", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20120511"}