lidocaine hydrochloride

Generic: lidocaine hydrochloride

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride
Generic Name lidocaine hydrochloride
Labeler hf acquisition co llc, dba healthfirst
Dosage Form JELLY
Routes
TOPICAL
Active Ingredients

lidocaine hydrochloride 20 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1552
Product ID 51662-1552_1035721c-e0f9-34b3-e063-6294a90aa4a5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA086283
Listing Expiration 2026-12-31
Marketing Start 2021-06-14

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621552
Hyphenated Format 51662-1552

Supplemental Identifiers

RxCUI
1011852
UNII
V13007Z41A

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 (source: ndc)
Generic Name lidocaine hydrochloride (source: ndc)
Application Number ANDA086283 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 25 POUCH in 1 CASE (51662-1552-3) / 1 CARTON in 1 POUCH (51662-1552-2) / 1 VIAL, SINGLE-USE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

Ingredients (1)

lidocaine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "1035721c-e0f9-34b3-e063-6294a90aa4a5", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1011852"], "spl_set_id": ["c4c0df51-cc37-323d-e053-2995a90a154a"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CASE (51662-1552-3)  / 1 CARTON in 1 POUCH (51662-1552-2)  / 1 VIAL, SINGLE-USE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-USE", "package_ndc": "51662-1552-3", "marketing_start_date": "20210614"}], "brand_name": "LIDOCAINE HYDROCHLORIDE", "product_id": "51662-1552_1035721c-e0f9-34b3-e063-6294a90aa4a5", "dosage_form": "JELLY", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "51662-1552", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA086283", "marketing_category": "ANDA", "marketing_start_date": "20210614", "listing_expiration_date": "20261231"}