Package 72162-1098-2
Brand: lidocaine hydrochloride
Generic: lidocaine hydrochloridePackage Facts
Identity
Package NDC
72162-1098-2
Digits Only
7216210982
Product NDC
72162-1098
Description
1 BOTTLE in 1 CARTON (72162-1098-2) / 50 mL in 1 BOTTLE
Marketing
Marketing Status
Brand
lidocaine hydrochloride
Generic
lidocaine hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "69a49b4b-2d3d-400f-8710-49029a33fbfe", "openfda": {"unii": ["EC2CNF7XFP"], "rxcui": ["1010878"], "spl_set_id": ["ed43f2c3-606c-4998-8fca-ee9b13cd18db"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (72162-1098-2) / 50 mL in 1 BOTTLE", "package_ndc": "72162-1098-2", "marketing_start_date": "20230926"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "72162-1098_69a49b4b-2d3d-400f-8710-49029a33fbfe", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "72162-1098", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": "40 mg/mL"}], "application_number": "ANDA040710", "marketing_category": "ANDA", "marketing_start_date": "20070227", "listing_expiration_date": "20261231"}