lidocaine hydrochloride
Generic: lidocaine hydrochloride
Labeler: b. braun medical inc.Drug Facts
Product Profile
Brand Name
lidocaine hydrochloride
Generic Name
lidocaine hydrochloride
Labeler
b. braun medical inc.
Dosage Form
INJECTION
Routes
Active Ingredients
lidocaine hydrochloride anhydrous 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0264-9376
Product ID
0264-9376_21658976-c912-45c1-9969-2fa865576b81
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208474
Listing Expiration
2026-12-31
Marketing Start
2018-08-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
02649376
Hyphenated Format
0264-9376
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA208474 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 5 AMPULE in 1 CARTON (0264-9376-88) / 5 mL in 1 AMPULE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION"], "spl_id": "21658976-c912-45c1-9969-2fa865576b81", "openfda": {"unii": ["EC2CNF7XFP"], "rxcui": ["1737566"], "spl_set_id": ["e0e479e6-4c94-44d0-8074-d0ee7b2bde22"], "manufacturer_name": ["B. Braun Medical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 AMPULE in 1 CARTON (0264-9376-88) / 5 mL in 1 AMPULE", "package_ndc": "0264-9376-88", "marketing_start_date": "20180803"}], "brand_name": "LIDOCAINE HYDROCHLORIDE", "product_id": "0264-9376_21658976-c912-45c1-9969-2fa865576b81", "dosage_form": "INJECTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "0264-9376", "generic_name": "LIDOCAINE HYDROCHLORIDE", "labeler_name": "B. Braun Medical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LIDOCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE ANHYDROUS", "strength": "10 mg/mL"}], "application_number": "ANDA208474", "marketing_category": "ANDA", "marketing_start_date": "20180803", "listing_expiration_date": "20261231"}