NDC 72162-1346 – Buprenorphine and Naloxone
Buprenorphine Hydrochloride 2 mg/1; Naloxone Hydrochloride Dihydrate .5 mg/1 · Tablet · Sublingual
Product NDC72162-1346
Product details
- Brand name
- Buprenorphine and Naloxone
- Generic name
- Buprenorphine and Naloxone
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA205601
- Marketed since
- April 13, 2020
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 2 mg/1
- Naloxone Hydrochloride Dihydrate .5 mg/1
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1346-3 | 30 TABLET in 1 BOTTLE, PLASTIC (72162-1346-3) | Apr 3, 2026 |
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