lidocaine hydrochloride

Generic: lidocaine hydrochloride

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride
Generic Name lidocaine hydrochloride
Labeler preferred pharmaceuticals inc.
Dosage Form SOLUTION
Routes
ORAL TOPICAL
Active Ingredients

lidocaine hydrochloride 20 mg/mL

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8507
Product ID 68788-8507_4aee6a9c-0a4b-41c6-a6ff-a9b3d4f1f620
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216780
Listing Expiration 2026-12-31
Marketing Start 2023-08-16

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 687888507
Hyphenated Format 68788-8507

Supplemental Identifiers

RxCUI
1010739
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 ANDA216780 (source: ndc)
Routes
ORAL TOPICAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 100 mL in 1 BOTTLE (68788-8507-1)
source: ndc

Packages (1)

68788-8507-1 100 mL in 1 BOTTLE (68788-8507-1)

Ingredients (1)

lidocaine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Lidocaine hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL", "TOPICAL"], "spl_id": "4aee6a9c-0a4b-41c6-a6ff-a9b3d4f1f620", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["55aa77b8-7601-4432-8631-bfec58daf247"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 mL in 1 BOTTLE (68788-8507-1)", "package_ndc": "68788-8507-1", "marketing_start_date": "20230816"}], "brand_name": "Lidocaine hydrochloride", "product_id": "68788-8507_4aee6a9c-0a4b-41c6-a6ff-a9b3d4f1f620", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "68788-8507", "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": "ANDA216780", "marketing_category": "ANDA", "marketing_start_date": "20230816", "listing_expiration_date": "20261231"}