cocaine hydrochloride

Generic: cocaine hydrochloride

Labeler: lxo us inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA AUTHORIZED GENERIC Inactive Finished

Drug Facts

Product Profile

Brand Name cocaine hydrochloride
Generic Name cocaine hydrochloride
Labeler lxo us inc.
Dosage Form SOLUTION
Routes
NASAL
Active Ingredients

cocaine hydrochloride 40 mg/mL

Manufacturer
LXO US INC.

Identifiers & Regulatory

Product NDC 70839-362
Product ID 70839-362_0fb0298f-9757-26e8-e063-6294a90ae8f2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA AUTHORIZED GENERIC
Application Number NDA209963
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2024-01-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70839362
Hyphenated Format 70839-362

Supplemental Identifiers

RxCUI
1995288
UNII
XH8T8T6WZH

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cocaine hydrochloride (source: ndc)
Generic Name cocaine hydrochloride (source: ndc)
Application Number NDA209963 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/mL
source: ndc
Packaging
  • 1 BOTTLE, GLASS in 1 CARTON (70839-362-04) / 4 mL in 1 BOTTLE, GLASS
source: ndc

Packages (1)

Ingredients (1)

cocaine hydrochloride (40 mg/mL)

Linked Drug Pages (1)

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"}