Package 76420-351-30

Brand: eha

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-351-30
Digits Only 7642035130
Product NDC 76420-351
Product ID 76420-351_7d77ecf6-5731-d43e-e053-2991aa0af0db
Description

88 mL in 1 BOTTLE (76420-351-30)

Marketing

Marketing Status
Marketed Since 2016-06-07
Brand eha
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Eha ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "7d77ecf6-5731-d43e-e053-2991aa0af0db", "openfda": {"upc": ["0376420351306"], "unii": ["V13007Z41A"], "spl_set_id": ["09835640-55c3-4bfa-9ad3-15d37f06e871"], "manufacturer_name": ["Asclemed USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "88 mL in 1 BOTTLE (76420-351-30)", "package_ndc": "76420-351-30", "marketing_start_date": "20160607"}], "brand_name": "Eha", "product_id": "76420-351_7d77ecf6-5731-d43e-e053-2991aa0af0db", "dosage_form": "LOTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "76420-351", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eha", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "4 g/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160607", "listing_expiration_date": "20261231"}