lidocaine hydrochloride

Generic: lidocaine hydrochloride

Labeler: northstar rxllc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride
Generic Name lidocaine hydrochloride
Labeler northstar rxllc
Dosage Form INJECTION, SOLUTION
Routes
INFILTRATION PERINEURAL
Active Ingredients

lidocaine hydrochloride anhydrous 20 mg/mL

Manufacturer
NorthStar RxLLC

Identifiers & Regulatory

Product NDC 72603-825
Product ID 72603-825_2e79ebee-c652-5f99-e063-6294a90a44ac
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214336
Listing Expiration 2026-12-31
Marketing Start 2025-02-01

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 72603825
Hyphenated Format 72603-825

Supplemental Identifiers

RxCUI
1010033 1010671
UPC
0372603744019 0372603722017 0372603825015 0372603732016
UNII
EC2CNF7XFP

Packaging Origin

Original Packager
true

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 ANDA214336 (source: ndc)
Routes
INFILTRATION PERINEURAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 10 VIAL, MULTI-DOSE in 1 CARTON (72603-825-10) / 50 mL in 1 VIAL, MULTI-DOSE (72603-825-01)
  • 25 VIAL, MULTI-DOSE in 1 CARTON (72603-825-25) / 50 mL in 1 VIAL, MULTI-DOSE (72603-825-01)
source: ndc

Packages (2)

Ingredients (1)

lidocaine hydrochloride anhydrous (20 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION", "PERINEURAL"], "spl_id": "2e79ebee-c652-5f99-e063-6294a90a44ac", "openfda": {"upc": ["0372603744019", "0372603722017", "0372603825015", "0372603732016"], "unii": ["EC2CNF7XFP"], "rxcui": ["1010033", "1010671"], "spl_set_id": ["6a7fa6c5-b550-46ac-99a3-5c49339e6dbd"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 CARTON (72603-825-10)  / 50 mL in 1 VIAL, MULTI-DOSE (72603-825-01)", "package_ndc": "72603-825-10", "marketing_start_date": "20250201"}, {"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (72603-825-25)  / 50 mL in 1 VIAL, MULTI-DOSE (72603-825-01)", "package_ndc": "72603-825-25", "marketing_start_date": "20250201"}], "brand_name": "Lidocaine hydrochloride", "product_id": "72603-825_2e79ebee-c652-5f99-e063-6294a90a44ac", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "72603-825", "generic_name": "Lidocaine hydrochloride", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": "20 mg/mL"}], "application_number": "ANDA214336", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}