NDC 67877-606 – Buprenorphine And Naloxone
Buprenorphine Hydrochloride 8 mg/1; Naloxone Hydrochloride 2 mg/1 · Tablet · Sublingual
Product NDC67877-606
Product details
- Brand name
- Buprenorphine And Naloxone
- Generic name
- Buprenorphine And Naloxone
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA214930
- Marketed since
- July 3, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 8 mg/1
- Naloxone Hydrochloride 2 mg/1
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 67877-606-30 | 30 TABLET in 1 BOTTLE (67877-606-30) | Jul 3, 2026 |
| 67877-606-84 | 3 BLISTER PACK in 1 CARTON (67877-606-84) / 10 TABLET in 1 BLISTER PACK | Jul 3, 2026 |
| 67877-606-90 | 90 TABLET in 1 BOTTLE (67877-606-90) | Jul 3, 2026 |
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