NDC 65162-416 – Buprenorphine HCl and Naloxone HCl
Buprenorphine Hydrochloride 2 mg/1; Naloxone Hydrochloride Dihydrate .5 mg/1 · Tablet · Sublingual
Product NDC65162-416
Product details
- Brand name
- Buprenorphine HCl and Naloxone HCl
- Generic name
- Buprenorphine and Naloxone
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA203136
- Marketed since
- February 22, 2013
- 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 HCl and Naloxone HCl →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 65162-416-03 | 30 TABLET in 1 BOTTLE (65162-416-03) | Feb 22, 2013 |
| 65162-416-09 | 90 TABLET in 1 BOTTLE (65162-416-09) | Feb 22, 2013 |
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