NDC 31722-482 – Buprenorphine and Naloxone
Buprenorphine Hydrochloride 12 mg/1; Naloxone Hydrochloride 3 mg/1 · Film, Soluble · Buccal, Sublingual
Product NDC31722-482
Product details
- Brand name
- Buprenorphine and Naloxone
- Generic name
- Buprenorphine and naloxone
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Film, Soluble
- Route
- Buccal, Sublingual
- Marketing category
- ANDA · ANDA219850
- Marketed since
- May 1, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
- Buprenorphine Hydrochloride 12 mg/1
- Naloxone Hydrochloride 3 mg/1
Uses, dosage, side effects and warnings for Buprenorphine and Naloxone →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 31722-482-30 | 30 POUCH in 1 CARTON (31722-482-30) / 1 FILM, SOLUBLE in 1 POUCH (31722-482-31) | May 1, 2026 |
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