Package 51662-1651-1

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1651-1
Digits Only 5166216511
Product NDC 51662-1651
Description

5 mL in 1 VIAL, SINGLE-DOSE (51662-1651-1)

Marketing

Marketing Status
Marketed Since 2013-03-14
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "1b584ef0-3664-0d2a-e063-6394a90a1757", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737566"], "spl_set_id": ["1b584ef0-3663-0d2a-e063-6394a90a1757"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-DOSE (51662-1651-1)", "package_ndc": "51662-1651-1", "marketing_start_date": "20130314"}], "brand_name": "LIDOCAINE HYDROCHLORIDE", "product_id": "51662-1651_1b584ef0-3664-0d2a-e063-6394a90a1757", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "51662-1651", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA203082", "marketing_category": "ANDA", "marketing_start_date": "20130314", "listing_expiration_date": "20261231"}