lidocaine

Generic: lidocaine

Labeler: puretek corporation
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name lidocaine
Generic Name lidocaine
Labeler puretek corporation
Dosage Form PATCH
Routes
TOPICAL
Active Ingredients

lidocaine 50 mg/g

Manufacturer
PureTek Corporation

Identifiers & Regulatory

Product NDC 59088-396
Product ID 59088-396_45c9f4a4-9398-4268-e063-6394a90a651f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA200675
Listing Expiration 2026-12-31
Marketing Start 2013-09-15

Pharmacologic Class

Established (EPC)
amide local anesthetic [epc] antiarrhythmic [epc]
Chemical Structure
amides [cs]
Physiologic Effect
local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 59088396
Hyphenated Format 59088-396

Supplemental Identifiers

RxCUI
1745091
UNII
98PI200987
NUI
N0000175682 M0000897 N0000175426 N0000175976

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 (source: ndc)
Generic Name lidocaine (source: ndc)
Application Number ANDA200675 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/g
source: ndc
Packaging
  • HOW SUPPLIED Lidocaine patch 5% is available as the following: Carton of 15 patches, NDC 59088-396-82 Carton of 30 patches, NDC 59088-396-54 Each patch is packaged into an individual child-resistant envelope. Store at 20 o to 25 o C (68 o to 77 o F) [See USP Controlled Room Temperature]. For more information, call Actavis at 1-800-272-5525. Manufactured by: Actavis Laboratories UT, Inc. Salt Lake City, UT 84108 USA Distributed by: PureTek Corporation San Fernando, CA 91340 USA Rev. 37780 02/16
  • PRINCIPAL DISPLAY PANEL NDC 59088-396-54 Lidocaine Patch 5% Rx only 30 Patches (30 Envelopes Containing 1 Patch Each) label
source: label

Packages (0)

No package records.

Ingredients (1)

lidocaine (50 mg/g)

Linked Drug Pages (1)

Lidocaine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "45c9f4a4-9398-4268-e063-6394a90a651f", "openfda": {"nui": ["N0000175682", "M0000897", "N0000175426", "N0000175976"], "unii": ["98PI200987"], "rxcui": ["1745091"], "spl_set_id": ["85e72943-6989-42f4-b519-a3ebbf4bc777"], "pharm_class_cs": ["Amides [CS]"], "pharm_class_pe": ["Local Anesthesia [PE]"], "pharm_class_epc": ["Amide Local Anesthetic [EPC]", "Antiarrhythmic [EPC]"], "manufacturer_name": ["PureTek Corporation"]}, "finished": true, "packaging": [], "brand_name": "Lidocaine", "product_id": "59088-396_45c9f4a4-9398-4268-e063-6394a90a651f", "dosage_form": "PATCH", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-396", "generic_name": "Lidocaine", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lidocaine", "active_ingredients": [{"name": "LIDOCAINE", "strength": "50 mg/g"}], "application_number": "ANDA200675", "marketing_category": "ANDA", "marketing_start_date": "20130915", "listing_expiration_date": "20261231"}