NDCFind

Buprenorphine 58118-0502-08

Package NDC

58118-0502-08

Product NDC: 58118-0502

Manufacturer
Clinical Solutions Wholesale, Llc
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
October 25, 2017
Listing Expires
December 31, 2026
Application
ANDA207276

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

58118-0502-08Selected

30 TABLET in 1 BLISTER PACK (58118-0502-8)