lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
preferred pharmaceuticals inc.
Dosage Form
SOLUTION
Routes
Active Ingredients
lidocaine hydrochloride 20 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8847
Product ID
68788-8847_abf60c5c-66df-4894-aa8f-bf770a6e9d00
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218138
Listing Expiration
2026-12-31
Marketing Start
2025-03-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888847
Hyphenated Format
68788-8847
Supplemental Identifiers
RxCUI
UNII
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
ANDA218138 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/mL
Packaging
- 100 mL in 1 BOTTLE (68788-8847-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "abf60c5c-66df-4894-aa8f-bf770a6e9d00", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["abf60c5c-66df-4894-aa8f-bf770a6e9d00"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8847-1)", "package_ndc": "68788-8847-1", "marketing_start_date": "20250324"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "68788-8847_abf60c5c-66df-4894-aa8f-bf770a6e9d00", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "68788-8847", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA218138", "marketing_category": "ANDA", "marketing_start_date": "20250324", "listing_expiration_date": "20261231"}