Package 70839-359-04

Brand: goprelto

Generic: cocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70839-359-04
Digits Only 7083935904
Product NDC 70839-359
Product ID 70839-359_0f897764-fe31-090a-e063-6294a90af106
Description

1 BOTTLE, GLASS in 1 CARTON (70839-359-04) / 4 mL in 1 BOTTLE, GLASS

Marketing

Marketing Status
Marketed Since 2024-02-09
Brand goprelto
Generic cocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

Goprelto ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "0f897764-fe31-090a-e063-6294a90af106", "openfda": {"unii": ["XH8T8T6WZH"], "rxcui": ["1995288", "1995293"], "spl_set_id": ["0f897764-fe30-090a-e063-6294a90af106"], "manufacturer_name": ["LXO US Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (70839-359-04)  / 4 mL in 1 BOTTLE, GLASS", "package_ndc": "70839-359-04", "marketing_start_date": "20240209"}], "brand_name": "Goprelto", "product_id": "70839-359_0f897764-fe31-090a-e063-6294a90af106", "dosage_form": "SOLUTION", "product_ndc": "70839-359", "dea_schedule": "CII", "generic_name": "cocaine hydrochloride", "labeler_name": "LXO US Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Goprelto", "active_ingredients": [{"name": "COCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "NDA209963", "marketing_category": "NDA", "marketing_start_date": "20240209", "listing_expiration_date": "20261231"}