NDC 70518-4570 – Buprenorphine hydrochloride
Buprenorphine Hydrochloride 2 mg/1 · Tablet · Sublingual
Product NDC70518-4570
Product details
- Brand name
- Buprenorphine hydrochloride
- Generic name
- Buprenorphine hydrochloride
- Labeler
- REMEDYREPACK INC.
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA090279
- Marketed since
- February 10, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 2 mg/1
Uses, dosage, side effects and warnings for Buprenorphine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70518-4570-0 | 30 POUCH in 1 BOX (70518-4570-0) / 1 TABLET in 1 POUCH (70518-4570-1) | Feb 10, 2026 |
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