morphine sulfate

Generic: morphine sulfate

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name morphine sulfate
Generic Name morphine sulfate
Labeler actavis pharma, inc.
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

morphine sulfate 30 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0228-4271
Product ID 0228-4271_7caa4c88-b5f3-410b-a824-87916d6c7655
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203849
DEA Schedule cii
Marketing Start 2015-10-26
Marketing End 2026-07-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02284271
Hyphenated Format 0228-4271

Supplemental Identifiers

RxCUI
891874 891881 891888 891893 892646
UNII
X3P646A2J0

Packaging Origin

Original Packager
true

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 ANDA203849 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-4271-11)
source: ndc

Packages (1)

0228-4271-11 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-4271-11)

Ingredients (1)

morphine sulfate (30 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": "7caa4c88-b5f3-410b-a824-87916d6c7655", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["891874", "891881", "891888", "891893", "892646"], "spl_set_id": ["75fb4282-0bbd-4d63-a7d1-5142780a4fae"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0228-4271-11)", "package_ndc": "0228-4271-11", "marketing_end_date": "20260731", "marketing_start_date": "20151026"}], "brand_name": "Morphine sulfate", "product_id": "0228-4271_7caa4c88-b5f3-410b-a824-87916d6c7655", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0228-4271", "dea_schedule": "CII", "generic_name": "Morphine sulfate", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "30 mg/1"}], "application_number": "ANDA203849", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20151026"}