NDC 50090-7559 – Buprenorphine hydrochloride
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC50090-7559
Product details
- Brand name
- Buprenorphine hydrochloride
- Generic name
- Buprenorphine hydrochloride
- Labeler
- A-S Medication Solutions
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA090622
- Marketed since
- October 12, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 8 mg/1
Uses, dosage, side effects and warnings for Buprenorphine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 50090-7559-0 | 30 TABLET in 1 BOTTLE (50090-7559-0) | May 27, 2025 |
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