Package 67877-670-01
Brand: morphine sulfate
Generic: morphine sulfatePackage Facts
Identity
Package NDC
67877-670-01
Digits Only
6787767001
Product NDC
67877-670
Description
100 TABLET in 1 BOTTLE (67877-670-01)
Marketing
Marketing Status
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": "2d263950-4148-405d-b582-13857ac88044", "openfda": {"upc": ["0367877671017"], "unii": ["X3P646A2J0"], "rxcui": ["892582", "892672"], "spl_set_id": ["07593aa4-f2c4-4d6e-b186-ab2a4ecaa38a"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-670-01)", "package_ndc": "67877-670-01", "marketing_start_date": "20210211"}], "brand_name": "MORPHINE SULFATE", "product_id": "67877-670_2d263950-4148-405d-b582-13857ac88044", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "67877-670", "dea_schedule": "CII", "generic_name": "MORPHINE SULFATE", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MORPHINE SULFATE", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "15 mg/1"}], "application_number": "ANDA212451", "marketing_category": "ANDA", "marketing_start_date": "20210211", "listing_expiration_date": "20261231"}