Package 51662-1471-1

Brand: propofol

Generic: propofol
NDC Package

Package Facts

Identity

Package NDC 51662-1471-1
Digits Only 5166214711
Product NDC 51662-1471
Product ID 51662-1471_2b39daef-65e6-0aa7-e063-6394a90a364d
Description

50 mL in 1 VIAL (51662-1471-1)

Marketing

Marketing Status
Marketed Since 2019-12-15
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": "2b39daef-65e6-0aa7-e063-6394a90a364d", "openfda": {"nui": ["N0000175975", "N0000175681"], "unii": ["YI7VU623SF"], "rxcui": ["1808222"], "spl_set_id": ["99c8438a-2b3c-796e-e053-2a95a90a0200"], "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": "50 mL in 1 VIAL (51662-1471-1)", "package_ndc": "51662-1471-1", "marketing_start_date": "20191215"}], "brand_name": "PROPOFOL", "product_id": "51662-1471_2b39daef-65e6-0aa7-e063-6394a90a364d", "dosage_form": "INJECTION, EMULSION", "pharm_class": ["General Anesthesia [PE]", "General Anesthetic [EPC]"], "product_ndc": "51662-1471", "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": "20191215", "listing_expiration_date": "20261231"}