Buprenorphine Hydrochloride 50090-7559
Product NDC
50090-7559- Manufacturer
- A-S Medication Solutions
- Dosage Form
- Tablet
- Route
- Sublingual
- Product Type
- Human Prescription Drug
- DEA Schedule
- Schedule CIII
- Marketing Start
- October 12, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA090622
Active Ingredients
| Ingredient | Strength |
|---|---|
| Buprenorphine Hydrochloride | 8 mg/1 |
Drug Class
Partial Opioid Agonist [EPC]Partial Opioid Agonists [MoA]
Packaging Options(1)
30 TABLET in 1 BOTTLE (50090-7559-0)