lidocaine hydrochloride and dextrose

Generic: lidocaine hydrochloride and dextrose

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

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride and dextrose
Generic Name lidocaine hydrochloride and dextrose
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

lidocaine hydrochloride 8 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1657
Product ID 51662-1657_1bf999b5-e291-dcbd-e063-6294a90a2bab
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018461
Listing Expiration 2026-12-31
Marketing Start 1981-04-22

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 516621657
Hyphenated Format 51662-1657

Supplemental Identifiers

RxCUI
1737723
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 and dextrose (source: ndc)
Generic Name lidocaine hydrochloride and dextrose (source: ndc)
Application Number NDA018461 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 8 mg/mL
source: ndc
Packaging
  • 250 mL in 1 BAG (51662-1657-1)
source: ndc

Packages (1)

51662-1657-1 250 mL in 1 BAG (51662-1657-1)

Ingredients (1)

lidocaine hydrochloride (8 mg/mL)

Linked Drug Pages (1)

LIDOCAINE HYDROCHLORIDE AND DEXTROSE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "1bf999b5-e291-dcbd-e063-6294a90a2bab", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1737723"], "spl_set_id": ["1bf999b5-e290-dcbd-e063-6294a90a2bab"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "250 mL in 1 BAG (51662-1657-1)", "package_ndc": "51662-1657-1", "marketing_start_date": "19810422"}], "brand_name": "LIDOCAINE HYDROCHLORIDE AND DEXTROSE", "product_id": "51662-1657_1bf999b5-e291-dcbd-e063-6294a90a2bab", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "51662-1657", "generic_name": "LIDOCAINE HYDROCHLORIDE AND DEXTROSE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE AND DEXTROSE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "8 mg/mL"}], "application_number": "NDA018461", "marketing_category": "NDA", "marketing_start_date": "19810422", "listing_expiration_date": "20261231"}