NDC 72189-582 – Buprenorphine Sublingual C-III
Buprenorphine Hydrochloride 8 mg/1 · Tablet · Sublingual
Product NDC72189-582
Product details
- Brand name
- Buprenorphine Sublingual C-III
- Generic name
- Buprenorphine Sublingual C-III
- Labeler
- Direct_Rx
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA078633
- Marketed since
- October 15, 2024
- 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 Sublingual C-III →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72189-582-60 | 60 TABLET in 1 BOTTLE (72189-582-60) | Oct 15, 2024 |
Other Buprenorphine Sublingual C-III products
- 72189-580 Buprenorphine Hydrochloride 2 mg/1 · Tablet · Direct_Rx