Package 59088-371-07

Brand: dermacinrx lidotral

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59088-371-07
Digits Only 5908837107
Product NDC 59088-371
Product ID 59088-371_36a4cb7d-d1e8-4056-8344-c9f110820fcc
Description

1 TUBE in 1 CARTON (59088-371-07) / 85 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2015-12-03
Brand dermacinrx lidotral
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

DermacinRx Lidotral ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "36a4cb7d-d1e8-4056-8344-c9f110820fcc", "openfda": {"unii": ["V13007Z41A"], "rxcui": ["1723991", "1723996"], "spl_set_id": ["23efec58-67cc-418d-85f5-7ef156443cbf"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (59088-371-07)  / 85 g in 1 TUBE", "package_ndc": "59088-371-07", "marketing_start_date": "20151203"}], "brand_name": "DermacinRx Lidotral", "product_id": "59088-371_36a4cb7d-d1e8-4056-8344-c9f110820fcc", "dosage_form": "CREAM", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "59088-371", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DermacinRx Lidotral", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "38.8 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20151203", "listing_expiration_date": "20261231"}