NDCFind

Buprenorphine Hcl 00406-7018-03

Package NDC

00406-7018-03

Product NDC: 00406-7018

Manufacturer
Specgx Llc
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
January 19, 2026
Listing Expires
December 31, 2026
Application
ANDA218473

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

Partial Opioid Agonist [EPC]Partial Opioid Agonists [MoA]

Selected Package

00406-7018-03Selected

30 TABLET in 1 BOTTLE (0406-7018-03)