NDC 0406-8020 – Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
Buprenorphine Hydrochloride 8 mg/1; Naloxone Hydrochloride Dihydrate 2 mg/1 · Tablet · Sublingual
Product NDC0406-8020
Product details
- Brand name
- Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
- Generic name
- Buprenorphine Hydrochloride and Naloxone Hydrochloride Dihydrate
- Labeler
- SpecGx LLC
- Dosage form
- Tablet
- Route
- Sublingual
- Marketing category
- ANDA · ANDA207000
- Marketed since
- December 13, 2017
- Listing expires
- December 31, 2027
- Pharmacologic class
- Opioid Antagonist; Partial Opioid Agonist
Active ingredients
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0406-8020-03 | 30 TABLET in 1 BOTTLE, PLASTIC (0406-8020-03) | Dec 13, 2017 |
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