Buprenorphine 87441-0011
Product NDC
87441-0011- Manufacturer
- Unit Dose Solutions, Inc.
- Dosage Form
- Tablet
- Route
- Sublingual
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- June 17, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA207276
Active Ingredients
| Ingredient | Strength |
|---|---|
| Buprenorphine Hydrochloride | 2 mg/1 |
Drug Class
Partial Opioid Agonist [EPC]Partial Opioid Agonists [MoA]
Packaging Options(1)
30 TABLET in 1 BLISTER PACK (87441-011-01)