Package 51672-1411-3

Brand: lidocaine hydrochloride

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51672-1411-3
Digits Only 5167214113
Product NDC 51672-1411
Product ID 51672-1411_39623a94-8b8c-17c6-e063-6294a90a4c31
Description

1 BOTTLE in 1 CARTON (51672-1411-3) / 50 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2023-12-08
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": ["TOPICAL"], "spl_id": "39623a94-8b8c-17c6-e063-6294a90a4c31", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010878"], "spl_set_id": ["845b96c1-36a3-431f-8316-112ae881d934"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (51672-1411-3)  / 50 mL in 1 BOTTLE", "package_ndc": "51672-1411-3", "marketing_start_date": "20231208"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "51672-1411_39623a94-8b8c-17c6-e063-6294a90a4c31", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "51672-1411", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "ANDA218182", "marketing_category": "ANDA", "marketing_start_date": "20231208", "listing_expiration_date": "20261231"}