lidocaine hci
Generic: lidocaine hci
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
lidocaine hci
Generic Name
lidocaine hci
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
epinephrine 10 ug/mL, lidocaine hydrochloride 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1419
Product ID
51662-1419_37b6f90b-34b4-98c1-e063-6394a90a4a74
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089644
Listing Expiration
2026-12-31
Marketing Start
2019-10-18
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621419
Hyphenated Format
51662-1419
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
lidocaine hci (source: ndc)
Generic Name
lidocaine hci (source: ndc)
Application Number
ANDA089644 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 ug/mL
- 10 mg/mL
Packaging
- 30 mL in 1 VIAL, MULTI-DOSE (51662-1419-1)
- 25 POUCH in 1 CASE (51662-1419-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1419-2) / 30 mL in 1 VIAL, MULTI-DOSE
Packages (2)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "37b6f90b-34b4-98c1-e063-6394a90a4a74", "openfda": {"nui": ["N0000000209", "N0000000245", "N0000175552", "N0000175555", "N0000175570", "M0003647"], "unii": ["YKH834O4BH", "V13007Z41A"], "rxcui": ["1010751"], "spl_set_id": ["95309440-34ec-11fe-e053-2a95a90a1c90"], "pharm_class_cs": ["Catecholamines [CS]"], "pharm_class_epc": ["alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]", "Catecholamine [EPC]"], "pharm_class_moa": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 VIAL, MULTI-DOSE (51662-1419-1)", "package_ndc": "51662-1419-1", "marketing_start_date": "20191018"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1419-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1419-2) / 30 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "51662-1419-3", "marketing_start_date": "20230109"}], "brand_name": "LIDOCAINE HCI", "product_id": "51662-1419_37b6f90b-34b4-98c1-e063-6394a90a4a74", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Catecholamine [EPC]", "Catecholamines [CS]", "Local Anesthesia [PE]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "51662-1419", "generic_name": "LIDOCAINE HCI", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HCI", "active_ingredients": [{"name": "EPINEPHRINE", "strength": "10 ug/mL"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "application_number": "ANDA089644", "marketing_category": "ANDA", "marketing_start_date": "20191018", "listing_expiration_date": "20261231"}