Package 59651-943-01

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-943-01
Digits Only 5965194301
Product NDC 59651-943
Product ID 59651-943_ab461805-413a-4fb3-88a1-224e1c423084
Description

100 mL in 1 BOTTLE (59651-943-01)

Marketing

Marketing Status
Marketed Since 2025-07-29
Brand lidocaine hydrochloride
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

LIDOCAINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "TOPICAL"], "spl_id": "ab461805-413a-4fb3-88a1-224e1c423084", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["ab461805-413a-4fb3-88a1-224e1c423084"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (59651-943-01)", "package_ndc": "59651-943-01", "marketing_start_date": "20250729"}], "brand_name": "LIDOCAINE HYDROCHLORIDE", "product_id": "59651-943_ab461805-413a-4fb3-88a1-224e1c423084", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59651-943", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA219759", "marketing_category": "ANDA", "marketing_start_date": "20250729", "listing_expiration_date": "20261231"}