NDCFind

Buprenorphine 71335-3152-09

Package NDC

71335-3152-09

Product NDC: 71335-3152

Manufacturer
Bryant Ranch Prepack
Dosage Form
Tablet
Route
Sublingual
Product Type
Human Prescription Drug
DEA Schedule
Schedule CIII
Marketing Start
February 17, 2016
Listing Expires
December 31, 2027
Application
ANDA201760

Active Ingredients

IngredientStrength
Buprenorphine Hydrochloride8 mg/1

Drug Class

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

Selected Package

71335-3152-09Selected

14 TABLET in 1 BOTTLE (71335-3152-9)

Other packages for this product(9)

120 TABLET in 1 BOTTLE (71335-3152-0)

90 TABLET in 1 BOTTLE (71335-3152-1)

60 TABLET in 1 BOTTLE (71335-3152-2)

30 TABLET in 1 BOTTLE (71335-3152-3)

20 TABLET in 1 BOTTLE (71335-3152-4)

7 TABLET in 1 BOTTLE (71335-3152-5)

28 TABLET in 1 BOTTLE (71335-3152-6)

1 TABLET in 1 BOTTLE (71335-3152-7)

12 TABLET in 1 BOTTLE (71335-3152-8)