Package 0641-6040-01

Brand: infumorph 500

Generic: morphine sulfate
NDC Package

Package Facts

Identity

Package NDC 0641-6040-01
Digits Only 0641604001
Product NDC 0641-6040
Product ID 0641-6040_b1c060cb-5c5b-495f-90b5-044e04f2a3f2
Description

20 mL in 1 AMPULE (0641-6040-01)

Marketing

Marketing Status
Marketed Since 1984-09-18
Brand infumorph 500
Generic morphine sulfate
Sample Package No

Linked Drug Pages (1)

INFUMORPH 200, INFUMORPH 500 ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EPIDURAL", "INTRATHECAL"], "spl_id": "b1c060cb-5c5b-495f-90b5-044e04f2a3f2", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["892652", "1731522", "1731998", "1731999"], "spl_set_id": ["db9ac9e3-d761-4a99-9f34-4946ebe8f255"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 AMPULE (0641-6040-01)", "package_ndc": "0641-6040-01", "marketing_start_date": "19840918"}], "brand_name": "INFUMORPH 500", "product_id": "0641-6040_b1c060cb-5c5b-495f-90b5-044e04f2a3f2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6040", "dea_schedule": "CII", "generic_name": "morphine sulfate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "INFUMORPH 500", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "25 mg/mL"}], "application_number": "NDA018565", "marketing_category": "NDA", "marketing_start_date": "19840918", "listing_expiration_date": "20271231"}