Package 84549-005-25

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 84549-005-25
Digits Only 8454900525
Product NDC 84549-005
Description

5 mL in 1 VIAL (84549-005-25)

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": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "42df73b0-20ed-d1aa-e063-6294a90aa275", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737761"], "spl_set_id": ["42df73b0-20ee-d1aa-e063-6294a90aa275"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL (84549-005-25)", "package_ndc": "84549-005-25", "marketing_start_date": "20251010"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "84549-005_42df73b0-20ed-d1aa-e063-6294a90aa275", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "84549-005", "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": "ANDA217692", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}