NDCFind

Buprenorphine Hydrochloride 00121-2038-30

Package NDC

00121-2038-30

Product NDC: 00121-2038

Manufacturer
Pai Holdings, Llc Dba Pharmaceutical Associates, Inc. And Dba Pai Pharma
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
October 12, 2023
Listing Expires
December 31, 2027
Application
ANDA090622

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

00121-2038-30Selected

30 TABLET in 1 BOTTLE (0121-2038-30)