Package 70839-362-04

Brand: cocaine hydrochloride

Generic: cocaine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70839-362-04
Digits Only 7083936204
Product NDC 70839-362
Product ID 70839-362_0fb0298f-9757-26e8-e063-6294a90ae8f2
Description

1 BOTTLE, GLASS in 1 CARTON (70839-362-04) / 4 mL in 1 BOTTLE, GLASS

Marketing

Marketing Status
Marketed Since 2024-01-29
Brand cocaine hydrochloride
Generic cocaine hydrochloride
Sample Package No

Linked Drug Pages (1)

COCAINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["NASAL"], "spl_id": "0fb0298f-9757-26e8-e063-6294a90ae8f2", "openfda": {"unii": ["XH8T8T6WZH"], "rxcui": ["1995288"], "spl_set_id": ["0fb0298f-9756-26e8-e063-6294a90ae8f2"], "manufacturer_name": ["LXO US INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (70839-362-04)  / 4 mL in 1 BOTTLE, GLASS", "package_ndc": "70839-362-04", "marketing_start_date": "20240129"}], "brand_name": "COCAINE HYDROCHLORIDE", "product_id": "70839-362_0fb0298f-9757-26e8-e063-6294a90ae8f2", "dosage_form": "SOLUTION", "product_ndc": "70839-362", "dea_schedule": "CII", "generic_name": "COCAINE HYDROCHLORIDE", "labeler_name": "LXO US INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "COCAINE HYDROCHLORIDE", "active_ingredients": [{"name": "COCAINE HYDROCHLORIDE", "strength": "40 mg/mL"}], "application_number": "NDA209963", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20240129", "listing_expiration_date": "20261231"}