lidocaine hydrochloride and epinephrine
Generic: lidocaine hydrochloride and epinephrine
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride and epinephrine
Generic Name
lidocaine hydrochloride and epinephrine
Labeler
propharma distribution
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
epinephrine 10 ug/mL, lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84549-182
Product ID
84549-182_463ecfc4-b5fa-62dd-e063-6294a90a9404
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA089646
Listing Expiration
2026-12-31
Marketing Start
2005-06-23
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549182
Hyphenated Format
84549-182
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 hydrochloride and epinephrine (source: ndc)
Generic Name
lidocaine hydrochloride and epinephrine (source: ndc)
Application Number
ANDA089646 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 ug/mL
- 20 mg/mL
Packaging
- 50 mL in 1 VIAL, MULTI-DOSE (84549-182-03)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "463ecfc4-b5fa-62dd-e063-6294a90a9404", "openfda": {"nui": ["N0000000209", "N0000000245", "N0000175552", "N0000175555", "N0000175570", "M0003647"], "unii": ["YKH834O4BH", "V13007Z41A"], "rxcui": ["1010759"], "spl_set_id": ["43048b6b-3c83-eef4-e063-6294a90a34cb"], "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": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 VIAL, MULTI-DOSE (84549-182-03)", "package_ndc": "84549-182-03", "marketing_start_date": "20251010"}], "brand_name": "Lidocaine Hydrochloride and Epinephrine", "product_id": "84549-182_463ecfc4-b5fa-62dd-e063-6294a90a9404", "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": "84549-182", "generic_name": "LIDOCAINE HYDROCHLORIDE and EPINEPHRINE", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride and Epinephrine", "active_ingredients": [{"name": "EPINEPHRINE", "strength": "10 ug/mL"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA089646", "marketing_category": "ANDA", "marketing_start_date": "20050623", "listing_expiration_date": "20261231"}