Package 84549-066-05

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-066-05
Digits Only 8454906605
Product NDC 84549-066
Description

5 mL in 1 VIAL, SINGLE-DOSE (84549-066-05)

Marketing

Marketing Status
Marketed Since 2026-01-19
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": "48c18a90-9d54-d200-e063-6394a90a1271", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737761"], "spl_set_id": ["48c18a90-9d53-d200-e063-6394a90a1271"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-DOSE (84549-066-05)", "package_ndc": "84549-066-05", "marketing_start_date": "20260119"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "84549-066_48c18a90-9d54-d200-e063-6394a90a1271", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "84549-066", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA040078", "marketing_category": "ANDA", "marketing_start_date": "20050907", "listing_expiration_date": "20271231"}