lidocaine hydrochloride

Generic: lidocaine hydrochloride

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine hydrochloride
Generic Name lidocaine hydrochloride
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
EPIDURAL INFILTRATION INTRACAUDAL PERINEURAL
Active Ingredients

lidocaine hydrochloride 15 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-4776
Product ID 0409-4776_78818553-f818-42a1-81b9-e5a5a5da5a27
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA080408
Listing Expiration 2027-12-31
Marketing Start 2006-01-06

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 04094776
Hyphenated Format 0409-4776

Supplemental Identifiers

RxCUI
1010033 1010671 1010900 1737343 1737562 1737566 1737568 1737636 1737757 1737763
UNII
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 (source: ndc)
Generic Name lidocaine hydrochloride (source: ndc)
Application Number ANDA080408 (source: ndc)
Routes
EPIDURAL INFILTRATION INTRACAUDAL PERINEURAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/mL
source: ndc
Packaging
  • 25 AMPULE in 1 CARTON (0409-4776-01) / 20 mL in 1 AMPULE (0409-4776-10)
source: ndc

Packages (1)

0409-4776-01 25 AMPULE in 1 CARTON (0409-4776-01) / 20 mL in 1 AMPULE (0409-4776-10)

Ingredients (1)

lidocaine hydrochloride (15 mg/mL)

Linked Drug Pages (1)

Lidocaine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EPIDURAL", "INFILTRATION", "INTRACAUDAL", "PERINEURAL"], "spl_id": "78818553-f818-42a1-81b9-e5a5a5da5a27", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1010033", "1010671", "1010900", "1737343", "1737562", "1737566", "1737568", "1737636", "1737757", "1737763"], "spl_set_id": ["3b2dd84e-cee8-4e58-d494-395a65a353a0"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 AMPULE in 1 CARTON (0409-4776-01)  / 20 mL in 1 AMPULE (0409-4776-10)", "package_ndc": "0409-4776-01", "marketing_start_date": "20060106"}], "brand_name": "Lidocaine Hydrochloride", "product_id": "0409-4776_78818553-f818-42a1-81b9-e5a5a5da5a27", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0409-4776", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine Hydrochloride", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "15 mg/mL"}], "application_number": "ANDA080408", "marketing_category": "ANDA", "marketing_start_date": "20060106", "listing_expiration_date": "20271231"}