NDCFind

Buprenorphine Hydrochloride 50090-7559-00

Package NDC

50090-7559-00

Product NDC: 50090-7559

Manufacturer
A-S Medication Solutions
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
October 12, 2023
Listing Expires
December 31, 2026
Application
ANDA090622

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

50090-7559-00Selected

30 TABLET in 1 BOTTLE (50090-7559-0)