NDCFind

Buprenorphine 71335-0950-06

Package NDC

71335-0950-06

Product NDC: 71335-0950

Manufacturer
Bryant Ranch Prepack
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 Hydrochloride2 mg/1

Drug Class

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

Selected Package

71335-0950-06Selected

1 TABLET in 1 BOTTLE (71335-0950-6)

Other packages for this product(7)

60 TABLET in 1 BOTTLE (71335-0950-1)

90 TABLET in 1 BOTTLE (71335-0950-2)

30 TABLET in 1 BOTTLE (71335-0950-3)

7 TABLET in 1 BOTTLE (71335-0950-4)

28 TABLET in 1 BOTTLE (71335-0950-5)

12 TABLET in 1 BOTTLE (71335-0950-7)

120 TABLET in 1 BOTTLE (71335-0950-8)