Package 72162-1352-1
Brand: morphine sulfate extended release
Generic: morphine sulfatePackage Facts
Identity
Package NDC
72162-1352-1
Digits Only
7216213521
Product NDC
72162-1352
Description
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1352-1)
Marketing
Marketing Status
Brand
morphine sulfate extended release
Generic
morphine sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "92c14ecf-f054-4fb4-8985-5121b3baa3d3", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["892646"], "spl_set_id": ["c94d9da6-7a12-44ee-a38f-3323ee27842c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72162-1352-1)", "package_ndc": "72162-1352-1", "marketing_start_date": "20240207"}], "brand_name": "Morphine Sulfate Extended Release", "product_id": "72162-1352_92c14ecf-f054-4fb4-8985-5121b3baa3d3", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "72162-1352", "dea_schedule": "CII", "generic_name": "Morphine Sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine Sulfate", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA074769", "marketing_category": "ANDA", "marketing_start_date": "20110114", "listing_expiration_date": "20261231"}