Package 51662-1542-1

Brand: etomidate

Generic: etomidate
NDC Package

Package Facts

Identity

Package NDC 51662-1542-1
Digits Only 5166215421
Product NDC 51662-1542
Product ID 51662-1542_dc43b289-4f33-1c1e-e053-2995a90a3a23
Description

20 mL in 1 VIAL, SINGLE-DOSE (51662-1542-1)

Marketing

Marketing Status
Marketed Since 2022-04-09
Brand etomidate
Generic etomidate
Sample Package No

Linked Drug Pages (1)

ETOMIDATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "dc43b289-4f33-1c1e-e053-2995a90a3a23", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654008"], "spl_set_id": ["dc43b289-4f32-1c1e-e053-2995a90a3a23"], "pharm_class_pe": ["General Anesthesia [PE]"], "pharm_class_epc": ["General Anesthetic [EPC]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1542-1)", "package_ndc": "51662-1542-1", "marketing_start_date": "20220409"}], "brand_name": "ETOMIDATE", "product_id": "51662-1542_dc43b289-4f33-1c1e-e053-2995a90a3a23", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1542", "generic_name": "ETOMIDATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETOMIDATE", "active_ingredients": [{"name": "ETOMIDATE", "strength": "40 mg/20mL"}], "application_number": "ANDA206126", "marketing_category": "ANDA", "marketing_start_date": "20220409", "listing_expiration_date": "20261231"}