Package 0641-6020-10

Brand: duramorph

Generic: morphine sulfate
NDC Package

Package Facts

Identity

Package NDC 0641-6020-10
Digits Only 0641602010
Product NDC 0641-6020
Product ID 0641-6020_aa74af85-7068-4254-9a79-c7f3792044a6
Description

10 AMPULE in 1 CARTON (0641-6020-10) / 10 mL in 1 AMPULE (0641-6020-01)

Marketing

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

Linked Drug Pages (1)

Duramorph ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EPIDURAL", "INTRATHECAL", "INTRAVENOUS"], "spl_id": "aa74af85-7068-4254-9a79-c7f3792044a6", "openfda": {"unii": ["X3P646A2J0"], "rxcui": ["892473", "892489", "1728783", "1728800"], "spl_set_id": ["ebb18761-e5c4-4238-bb84-f9549f500210"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (0641-6020-10)  / 10 mL in 1 AMPULE (0641-6020-01)", "package_ndc": "0641-6020-10", "marketing_start_date": "19840918"}], "brand_name": "Duramorph", "product_id": "0641-6020_aa74af85-7068-4254-9a79-c7f3792044a6", "dosage_form": "INJECTION", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0641-6020", "dea_schedule": "CII", "generic_name": "morphine sulfate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Duramorph", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": ".5 mg/mL"}], "application_number": "NDA018565", "marketing_category": "NDA", "marketing_start_date": "19840918", "listing_expiration_date": "20271231"}