Package 84549-276-02

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-276-02
Digits Only 8454927602
Product NDC 84549-276
Description

50 mL in 1 VIAL, MULTI-DOSE (84549-276-02)

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": "463e2023-6fb6-2240-e063-6394a90a8391", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010033"], "spl_set_id": ["42caf92e-6fa9-5bd7-e063-6294a90a3904"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, MULTI-DOSE (84549-276-02)", "package_ndc": "84549-276-02", "marketing_start_date": "20251010"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "84549-276_463e2023-6fb6-2240-e063-6394a90a8391", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "84549-276", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA088299", "marketing_category": "ANDA", "marketing_start_date": "20050712", "listing_expiration_date": "20261231"}