Package 65219-445-10

Brand: etomidate

Generic: etomidate
NDC Package

Package Facts

Identity

Package NDC 65219-445-10
Digits Only 6521944510
Product NDC 65219-445
Description

10 VIAL, SINGLE-DOSE in 1 CARTON (65219-445-10) / 10 mL in 1 VIAL, SINGLE-DOSE (65219-445-01)

Marketing

Marketing Status
Marketed Since 2021-08-01
Brand etomidate
Generic etomidate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "30488a7e-ea9e-4a27-95a9-a07149c50282", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654006", "1654008"], "spl_set_id": ["d07efb9e-5264-461d-96d8-e11fa71c5751"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (65219-445-10)  / 10 mL in 1 VIAL, SINGLE-DOSE (65219-445-01)", "package_ndc": "65219-445-10", "marketing_start_date": "20210801"}], "brand_name": "Etomidate", "product_id": "65219-445_30488a7e-ea9e-4a27-95a9-a07149c50282", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "65219-445", "generic_name": "Etomidate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Etomidate", "active_ingredients": [{"name": "ETOMIDATE", "strength": "2 mg/mL"}], "application_number": "ANDA215028", "marketing_category": "ANDA", "marketing_start_date": "20210801", "listing_expiration_date": "20261231"}