Package 72162-1792-1

Brand: morphine sulfate

Generic: morphine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-1792-1
Digits Only 7216217921
Product NDC 72162-1792
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1792-1)

Marketing

Marketing Status
Marketed Since 2012-05-11
Brand morphine sulfate
Generic morphine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9a1ca529-8268-4be3-b03f-b2f2238cc9dc", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["892646"], "spl_set_id": ["9a1ca529-8268-4be3-b03f-b2f2238cc9dc"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1792-1)", "package_ndc": "72162-1792-1", "marketing_start_date": "20120511"}], "brand_name": "Morphine sulfate", "product_id": "72162-1792_9a1ca529-8268-4be3-b03f-b2f2238cc9dc", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1792", "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": "200 mg/1"}], "application_number": "ANDA078761", "marketing_category": "ANDA", "marketing_start_date": "20120511", "listing_expiration_date": "20261231"}