Package 51662-1634-1

Brand: etomidate injection, solution

Generic: etomidate injection, solution
NDC Package

Package Facts

Identity

Package NDC 51662-1634-1
Digits Only 5166216341
Product NDC 51662-1634
Description

10 mL in 1 VIAL, SINGLE-DOSE (51662-1634-1)

Marketing

Marketing Status
Marketed Since 2023-09-25
Brand etomidate injection, solution
Generic etomidate injection, solution
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0635683b-880b-0cd4-e063-6394a90ab73e", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["Z22628B598"], "rxcui": ["1654006"], "spl_set_id": ["0635683b-880a-0cd4-e063-6394a90ab73e"], "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": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1634-1)", "package_ndc": "51662-1634-1", "marketing_start_date": "20230925"}], "brand_name": "ETOMIDATE injection, solution", "product_id": "51662-1634_0635683b-880b-0cd4-e063-6394a90ab73e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1634", "generic_name": "ETOMIDATE injection, solution", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ETOMIDATE injection, solution", "active_ingredients": [{"name": "ETOMIDATE", "strength": "20 mg/10mL"}], "application_number": "ANDA206126", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}