Package 76420-715-01

Brand: accucaine

Generic: lidocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-715-01
Digits Only 7642071501
Product NDC 76420-715
Description

1 AMPULE in 1 CARTON (76420-715-01) / 5 mL in 1 AMPULE

Marketing

Marketing Status
Marketed Since 2016-02-01
Brand accucaine
Generic lidocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INFILTRATION"], "spl_id": "02db6c14-f841-85bd-e063-6294a90a3bf9", "openfda": {"unii": ["V13007Z41A"], "spl_set_id": ["584642a8-9bed-4d86-bfaf-99018c180e34"], "manufacturer_name": ["Asclemed USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 AMPULE in 1 CARTON (76420-715-01)  / 5 mL in 1 AMPULE", "package_ndc": "76420-715-01", "marketing_start_date": "20160201"}], "brand_name": "Accucaine", "product_id": "76420-715_02db6c14-f841-85bd-e063-6294a90a3bf9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "76420-715", "generic_name": "Lidocaine Hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Accucaine", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "10 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}