Package 63739-997-64

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63739-997-64
Digits Only 6373999764
Product NDC 63739-997
Description

1 BOTTLE in 1 CARTON (63739-997-64) / 50 mL in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2027-03-31
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0b1800c4-84d7-4c41-acf3-5f3e8f2e2a8c", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010878"], "spl_set_id": ["903cd7bd-6c3d-4068-bb24-e91b1ca1393d"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (63739-997-64)  / 50 mL in 1 BOTTLE", "package_ndc": "63739-997-64", "marketing_end_date": "20270331", "marketing_start_date": "20240627"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "63739-997_0b1800c4-84d7-4c41-acf3-5f3e8f2e2a8c", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "63739-997", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "ANDA204494", "marketing_category": "ANDA", "marketing_end_date": "20270331", "marketing_start_date": "20240627"}