lidocaine hydrochloride and dextrose

Generic: lidocaine hydrochloride anhydrous and dextrose monohydrate

Labeler: b. braun medical inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride and dextrose
Generic Name lidocaine hydrochloride anhydrous and dextrose monohydrate
Labeler b. braun medical inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

dextrose monohydrate 5 g/100mL, lidocaine hydrochloride anhydrous .8 g/100mL

Manufacturer
B. Braun Medical Inc.

Identifiers & Regulatory

Product NDC 0264-9598
Product ID 0264-9598_9e352802-107c-4f90-babe-4f69c7dc892e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019830
Listing Expiration 2027-12-31
Marketing Start 1992-04-08

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 02649598
Hyphenated Format 0264-9598

Supplemental Identifiers

RxCUI
1737723 1737742 1737744
UNII
EC2CNF7XFP LX22YL083G

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 dextrose (source: ndc)
Generic Name lidocaine hydrochloride anhydrous and dextrose monohydrate (source: ndc)
Application Number NDA019830 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 5 g/100mL
  • .8 g/100mL
source: ndc
Packaging
  • 24 CONTAINER in 1 CASE (0264-9598-20) / 250 mL in 1 CONTAINER
source: ndc

Packages (1)

0264-9598-20 24 CONTAINER in 1 CASE (0264-9598-20) / 250 mL in 1 CONTAINER

Ingredients (2)

dextrose monohydrate (5 g/100mL) lidocaine hydrochloride anhydrous (.8 g/100mL)

Linked Drug Pages (1)

Lidocaine Hydrochloride and Dextrose ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "9e352802-107c-4f90-babe-4f69c7dc892e", "openfda": {"unii": ["EC2CNF7XFP", "LX22YL083G"], "rxcui": ["1737723", "1737742", "1737744"], "spl_set_id": ["7dff29d9-522d-40eb-a9d9-42377912d640"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 CONTAINER in 1 CASE (0264-9598-20)  / 250 mL in 1 CONTAINER", "package_ndc": "0264-9598-20", "marketing_start_date": "19920408"}], "brand_name": "Lidocaine Hydrochloride and Dextrose", "product_id": "0264-9598_9e352802-107c-4f90-babe-4f69c7dc892e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0264-9598", "generic_name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS and DEXTROSE MONOHYDRATE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride and Dextrose", "active_ingredients": [{"name": "DEXTROSE MONOHYDRATE", "strength": "5 g/100mL"}, {"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": ".8 g/100mL"}], "application_number": "NDA019830", "marketing_category": "NDA", "marketing_start_date": "19920408", "listing_expiration_date": "20271231"}