NDC 70839-359 – Goprelto

Cocaine Hydrochloride 40 mg/mL · Solution · Nasal

Human Prescription Drug DEA schedule CII

Product NDC70839-359

Product details

Brand name
Goprelto
Generic name
Cocaine hydrochloride
Labeler
LXO US Inc.
Dosage form
Solution
Route
Nasal
Marketing category
NDA · NDA209963
Marketed since
February 9, 2024
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Goprelto →

Package NDC codes (1)

Package NDCDescriptionSince
70839-359-041 BOTTLE, GLASS in 1 CARTON (70839-359-04) / 4 mL in 1 BOTTLE, GLASSFeb 9, 2024