lidocaine hydrochloride

Generic: lidocaine hydrochloride

Labeler: atlantic biologicals corp.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride
Generic Name lidocaine hydrochloride
Labeler atlantic biologicals corp.
Dosage Form SOLUTION
Routes
ORAL TOPICAL
Active Ingredients

lidocaine hydrochloride 20 mg/mL

Manufacturer
Atlantic Biologicals Corp.

Identifiers & Regulatory

Product NDC 17856-8138
Product ID 17856-8138_401eca82-6f41-2006-e063-6394a90a6421
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216780
Listing Expiration 2026-12-31
Marketing Start 2023-03-28

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 178568138
Hyphenated Format 17856-8138

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
  • 50 CUP, UNIT-DOSE in 1 CASE (17856-8138-1) / 15 mL in 1 CUP, UNIT-DOSE
source: ndc

Packages (1)

17856-8138-1 50 CUP, UNIT-DOSE in 1 CASE (17856-8138-1) / 15 mL in 1 CUP, UNIT-DOSE

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": "401eca82-6f41-2006-e063-6394a90a6421", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010739"], "spl_set_id": ["401ecb6c-392b-1d74-e063-6294a90a4005"], "manufacturer_name": ["Atlantic Biologicals Corp."]}, "finished": true, "packaging": [{"sample": false, "description": "50 CUP, UNIT-DOSE in 1 CASE (17856-8138-1)  / 15 mL in 1 CUP, UNIT-DOSE", "package_ndc": "17856-8138-1", "marketing_start_date": "20251001"}], "brand_name": "Lidocaine hydrochloride", "product_id": "17856-8138_401eca82-6f41-2006-e063-6394a90a6421", "dosage_form": "SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "17856-8138", "generic_name": "Lidocaine hydrochloride", "labeler_name": "Atlantic Biologicals Corp.", "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": "20230328", "listing_expiration_date": "20261231"}