lidocaine hydrochloride and epinephrine bitartrate (42756-1030)

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride and epinephrine bitartrate

Generic Name lidocaine hydrochloride and epinephrine bitartrate

Labeler iq dental

Dosage Form INJECTION, SOLUTION

Routes

SUBMUCOSAL

Active Ingredients

epinephrine bitartrate .01 mg/mL, lidocaine hydrochloride 20 mg/mL

Manufacturer

IQ Dental

Identifiers & Regulatory

Product NDC 42756-1030

Product ID 42756-1030_00e156a7-2bd7-48a3-b87f-957792c307f5

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA088390

Listing Expiration 2026-12-31

Marketing Start 2011-11-07

Pharmacologic Class

Classes

adrenergic alpha-agonists [moa] adrenergic beta-agonists [moa] amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] catecholamine [epc] catecholamines [cs] local anesthesia [pe] alpha-adrenergic agonist [epc] beta-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 427561030

Hyphenated Format 42756-1030

Supplemental Identifiers

RxCUI

1293648

UNII

30Q7KI53AK V13007Z41A

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 and epinephrine bitartrate (source: ndc)

Generic Name lidocaine hydrochloride and epinephrine bitartrate (source: ndc)

Application Number ANDA088390 (source: ndc)

Routes

SUBMUCOSAL

source: ndc

Resolved Composition

Strengths

.01 mg/mL
20 mg/mL

source: ndc

Packaging

50 CARTRIDGE in 1 CARTON (42756-1030-5) / 1.7 mL in 1 CARTRIDGE

source: ndc

Packages (1)

42756-1030-5 50 CARTRIDGE in 1 CARTON (42756-1030-5) / 1.7 mL in 1 CARTRIDGE

Ingredients (2)

epinephrine bitartrate (.01 mg/mL) lidocaine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Lidocaine Hydrochloride and Epinephrine Bitartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["SUBMUCOSAL"], "spl_id": "00e156a7-2bd7-48a3-b87f-957792c307f5", "openfda": {"unii": ["30Q7KI53AK", "V13007Z41A"], "rxcui": ["1293648"], "spl_set_id": ["b1b09a84-7978-4380-9c40-a4bf837be637"], "manufacturer_name": ["IQ Dental"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 CARTRIDGE in 1 CARTON (42756-1030-5)  / 1.7 mL in 1 CARTRIDGE", "package_ndc": "42756-1030-5", "marketing_start_date": "20111107"}], "brand_name": "Lidocaine Hydrochloride and Epinephrine Bitartrate", "product_id": "42756-1030_00e156a7-2bd7-48a3-b87f-957792c307f5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Catecholamine [EPC]", "Catecholamines [CS]", "Local Anesthesia [PE]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "42756-1030", "generic_name": "Lidocaine Hydrochloride and Epinephrine Bitartrate", "labeler_name": "IQ Dental", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride and Epinephrine Bitartrate", "active_ingredients": [{"name": "EPINEPHRINE BITARTRATE", "strength": ".01 mg/mL"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA088390", "marketing_category": "ANDA", "marketing_start_date": "20111107", "listing_expiration_date": "20261231"}