lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: northstar rxllcDrug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
northstar rxllc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride anhydrous 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72603-732
Product ID
72603-732_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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72603732
Hyphenated Format
72603-732
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 25 VIAL, MULTI-DOSE in 1 CARTON (72603-732-25) / 50 mL in 1 VIAL, MULTI-DOSE (72603-732-01)
Packages (1)
Ingredients (1)
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": "25 VIAL, MULTI-DOSE in 1 CARTON (72603-732-25) / 50 mL in 1 VIAL, MULTI-DOSE (72603-732-01)", "package_ndc": "72603-732-25", "marketing_start_date": "20250201"}], "brand_name": "Lidocaine hydrochloride", "product_id": "72603-732_2e79ebee-c652-5f99-e063-6294a90a44ac", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "72603-732", "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": "10 mg/mL"}], "application_number": "ANDA214336", "marketing_category": "ANDA", "marketing_start_date": "20250201", "listing_expiration_date": "20261231"}