NDCFind

Buprenorphine Hcl 58118-0176

Product NDC

58118-0176
Manufacturer
Clinical Solutions Wholesale, Llc
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
October 8, 2009
Listing Expires
December 31, 2026
Application
ANDA078633

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride2 mg/1

Drug Class

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

Packaging Options(1)

30 TABLET in 1 BLISTER PACK (58118-0176-8)