NDCFind

Buprenorphine 50090-5805-00

Package NDC

50090-5805-00

Product NDC: 50090-5805

Manufacturer
A-S Medication Solutions
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
October 25, 2017
Listing Expires
December 31, 2027
Application
ANDA207276

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

50090-5805-00Selected

30 TABLET in 1 BOTTLE (50090-5805-0)