Package 51662-1470-1

Brand: propofol

Generic: propofol
NDC Package

Package Facts

Identity

Package NDC 51662-1470-1
Digits Only 5166214701
Product NDC 51662-1470
Product ID 51662-1470_2b39ae97-5968-1329-e063-6294a90a2259
Description

100 mL in 1 VIAL (51662-1470-1)

Marketing

Marketing Status
Marketed Since 2019-12-14
Brand propofol
Generic propofol
Sample Package No

Linked Drug Pages (1)

PROPOFOL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2b39ae97-5968-1329-e063-6294a90a2259", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["YI7VU623SF"], "rxcui": ["1808217"], "spl_set_id": ["99af9e0a-c268-84ca-e053-2a95a90a0a3e"], "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": "100 mL in 1 VIAL (51662-1470-1)", "package_ndc": "51662-1470-1", "marketing_start_date": "20191214"}], "brand_name": "PROPOFOL", "product_id": "51662-1470_2b39ae97-5968-1329-e063-6294a90a2259", "dosage_form": "INJECTION, EMULSION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1470", "generic_name": "PROPOFOL", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PROPOFOL", "active_ingredients": [{"name": "PROPOFOL", "strength": "10 mg/mL"}], "application_number": "ANDA077908", "marketing_category": "ANDA", "marketing_start_date": "20191214", "listing_expiration_date": "20261231"}