Package 84549-277-02

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-277-02
Digits Only 8454927702
Product NDC 84549-277
Description

50 mL in 1 VIAL, MULTI-DOSE (84549-277-02)

Marketing

Marketing Status
Marketed Since 2025-10-10
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "463e3815-f8c9-449a-e063-6394a90a6aa6", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010671"], "spl_set_id": ["42d9e4cf-ca73-ec6d-e063-6394a90ae937"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, MULTI-DOSE (84549-277-02)", "package_ndc": "84549-277-02", "marketing_start_date": "20251010"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "84549-277_463e3815-f8c9-449a-e063-6394a90a6aa6", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "84549-277", "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": "ANDA088327", "marketing_category": "ANDA", "marketing_start_date": "20050615", "listing_expiration_date": "20261231"}