Package 42858-804-01

Brand: morphine sulfate extended release

Generic: morphine sulfate
NDC Package

Package Facts

Identity

Package NDC 42858-804-01
Digits Only 4285880401
Product NDC 42858-804
Description

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42858-804-01)

Marketing

Marketing Status
Marketed Since 2011-01-14
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": "9af2bef8-f859-40eb-a60e-65474efe2f21", "openfda": {"upc": ["0342858803014", "0342858801010", "0342858802017", "0342858805018"], "unii": ["X3P646A2J0"], "rxcui": ["891874", "891881", "891888", "891893", "892646"], "spl_set_id": ["19c7d9cc-6ce2-4c5c-8c3f-c24fd3342804"], "manufacturer_name": ["Rhodes Pharmaceuticals L. P."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (42858-804-01)", "package_ndc": "42858-804-01", "marketing_start_date": "20110114"}], "brand_name": "Morphine Sulfate Extended Release", "product_id": "42858-804_9af2bef8-f859-40eb-a60e-65474efe2f21", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "42858-804", "dea_schedule": "CII", "generic_name": "Morphine Sulfate", "labeler_name": "Rhodes Pharmaceuticals L. P.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine Sulfate", "brand_name_suffix": "Extended Release", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "100 mg/1"}], "application_number": "ANDA074769", "marketing_category": "ANDA", "marketing_start_date": "20110114", "listing_expiration_date": "20271231"}