Package 76420-540-05

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-540-05
Digits Only 7642054005
Product NDC 76420-540
Description

5 mL in 1 VIAL, SINGLE-DOSE (76420-540-05)

Marketing

Marketing Status
Marketed Since 2023-03-02
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": "f5e688fe-a3a6-70a5-e053-2a95a90a2889", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737761"], "spl_set_id": ["55a8372e-70d6-4b70-ac95-5226d0f5812a"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, SINGLE-DOSE (76420-540-05)", "package_ndc": "76420-540-05", "marketing_start_date": "20230302"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "76420-540_f5e688fe-a3a6-70a5-e053-2a95a90a2889", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "76420-540", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA203082", "marketing_category": "ANDA", "marketing_start_date": "20130314", "listing_expiration_date": "20261231"}