Buprenorphine 71335-3152
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
| Ingredient | Strength |
|---|---|
| Buprenorphine Hydrochloride | 8 mg/1 |
Drug Class
Partial Opioid Agonist [EPC]Partial Opioid Agonists [MoA]
Packaging Options(10)
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)
14 TABLET in 1 BOTTLE (71335-3152-9)