NDC 70518-4571 – buprenorphine hydrochloride
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC70518-4571
Product details
- Brand name
- buprenorphine hydrochloride
- Generic name
- buprenorphine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA090622
- Marketed since
- February 10, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 8 mg/1
Uses, dosage, side effects and warnings for Buprenorphine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4571-0 | 30 POUCH in 1 BOX (70518-4571-0) / 1 TABLET in 1 POUCH (70518-4571-1) | Feb 10, 2026 |
| 70518-4571-2 | 50 POUCH in 1 BOX (70518-4571-2) / 1 TABLET in 1 POUCH (70518-4571-1) | Jul 7, 2026 |
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